Senior Scientist Resume Samples

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AK
A Konopelski
Alan
Konopelski
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+1 (555) 104 7304
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Phone
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Experience Experience
Philadelphia, PA
Senior Scientist
Philadelphia, PA
Fisher Group
Philadelphia, PA
Senior Scientist
  • Collaborating closely with Cell Line Development (CLD) and Downstream Process Development (DSP) groups to improve workflow efficiency and overall process yield
  • Supervises technical staff, including work assignments and performance and development management
  • Assist management in establishing new processes or methodologies to improve operational efficiencies
  • Proactively investigates and develops improvements to existing processes or develops new and improved processes
  • Develop and execute laboratory work plans for self and junior members of team, using customer milestones and Division/site performance standards and metrics
  • Work as a member of a team on product development efforts, as well as on independent development and improvement projects
  • Drives claims assessments and substantiation. Autonomously creates work plans and executes, including development of risk assessments and contingency plans
Chicago, IL
R&D Senior Scientist
Chicago, IL
Yost, Kihn and Bayer
Chicago, IL
R&D Senior Scientist
  • Collaborate with Marketing to develop, prioritize and execute project portfolio
  • Providing support to and deputise for the R&D Manager
  • Connect and use network to develop better and faster products & processes
  • Foster personal development growth with continuous coaching and feedback on career development as per the R&D Guiding Principles and Corporate Core Values
  • Execute clinical testing in support of new product and claims development
  • Development within Chocolate and commercialization of one or more product/process(es)
  • Independently leading / coordinating medium & large sized projects regarding x-cat ingredients and recipes productivity to support the crew sugar & sweetener agenda. Significantly impacts direction and quality of work done. Mobilizes necessary means in terms of time and personnel to achieve these objectives. Projects cover research, analysis, brief, bench-top evaluation through to plant trials, commercialization and launch
present
Los Angeles, CA
Senior Scientist, Translational Medicine
Los Angeles, CA
Huels, Purdy and Haley
present
Los Angeles, CA
Senior Scientist, Translational Medicine
present
  • Develop and review study proposals, manage relationships and critically review data from contract labs and academic collaborators
  • Manages and/or coordinates workflow on projects
  • Provides input and makes recommendations to research strategies
  • Assists in the development of disease specific strategy for Celgene (collaboration portion)
  • Knowledge of biomarker discovery and development: assay development/validation, clinical discovery of biomarkers, MoA research,knowledge of platforms
  • Extensive knowledge of mammalian cell culture, including standard cell biology techniques and, working knowledge of cellular signaling and ELISA assays
  • Evaluate and advise on clinical trial biomarker/exploratory endpoint strategies, collect and analyze patient data to inform clinical development
Education Education
Bachelor’s Degree in Chemistry
Bachelor’s Degree in Chemistry
University of California, San Diego
Bachelor’s Degree in Chemistry
Skills Skills
  • Strong attention to details, organized, excellent communication skills (written and verbal), problem solving skills, and ability to make timely decisions
  • Strong initiative, positive attitude, and ability to function effectively in a highly collaborative team environment
  • Proficient knowledge of Immunology to be reasonably self-directed in establishing immune-profiling assays in the context of tumorigenesis
  • An ability to understand the regulatory expectations for critical aspects of cell bank quality including clonality and stability
  • Excellent interpersonal skills and a can-do attitude, with strong collaboration skills and ability to thrive in a fast-paced, global environment
  • Excellent oral and written communication skills, and good presentation skills. Ability to work in a fast-paced, goal-oriented, team environment
  • Previous experience in designing and implementing structure/function studies and comparability studies is highly desirable
  • Good knowledge and experience to apply Quality by Design principles and statistical analysis tools to evaluate drug product process and manufacturing process
  • Good knowledge of: Chemistry, Math, basic Statistics
  • Strong attention to detail based on vigilance in the analysis to enable correct conclusions
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15 Senior Scientist resume templates

1

Senior Scientist Resume Examples & Samples

  • Able to follow written protocols for method validations, degradation and photo stability studies for OTC product development. Results must be evaluated and entered into reports for review and QA sign off
  • Knowledge of Product Stability regulations and FDA guidelines
  • Must have excellent communication skills to discuss and/or explain test results to management or formulation chemists on request
  • Must be able to understand and use analytical instrumentation in the laboratory including, HPLC, GC, GC/MS, Karl Fischer, FT-IR, ICP, Auto-titrator, SPF Analyzer and X-ray Fluorescence
  • Develop new analytical methods when necessary
  • Perform analytical testing to support formulation chemists and solve critical R&D issues
  • M.S. Degree in Chemistry
  • Five years industrial experience
  • Proficiency in the use of wet chemistry techniques
  • Proficiency in analytical instrumentation including HPLC, UPLC, LC/MS, GC, GC/MS, In-Vitro SPF, Karl Fischer, FT-IR, ICP and XRF
  • Proficiency in FDA Regulations and ICH Guidelines
2

Senior Scientist Resume Examples & Samples

  • Builds Collaborative Relationships: Will need to work closes with Market Research, Product Development, and product formulators. Will need to work closely with suppliers to source new fats and oils with appropriate qualities and lipid profiles
  • Drives Creativity and Innovation
  • Independence of Action and Accountability - In this role, the R&D person would be responsible for setting technical direction to meet required benefits and aesthetics. Independence is desired so that the R&D person can directly collaborate with other functions and 3rd parties
  • Decision Making - This person would be responsible for formulation decisions both at the bench and with 3rd party manufacturers
  • Leadership - Currently this role does not have any direct reports. Role requires individual leadership, collaboration, and some project management skills
  • 5-8 years of experience Work history in the food or personal care industry focused on fats and oils
3

Senior Scientist Resume Examples & Samples

  • 70 % Develop and implement strategies for the identification, development and characterization of histopathological features of animal models. Support to multiple ongoing projects, including relevance to human disease and translational biomarkers
  • Responsible for identifying and validating novel histopathologic methods to assist on biomarker identification and drug development
  • Assessment and interpretation of morphologic changes and clinical pathology data from animal studies, using pathological biomarkers to define the mechanism of action in support of drug development
  • Participate in the planning and execution of experiments while providing pathology and histology expertise to multiple projects across the Department
  • 30% Perform in depth literature searches. Understand current concepts in the field
  • Responsible for the preparation and distribution of study reports including conclusions and recommendations
  • Participate in cross-functional project teams, meetings, seminars and conferences in support of research goals
4

Senior Scientist Early Clinical Resume Examples & Samples

  • Manage the CRO relationship for Clinical Trials
  • Writing and editing of the clinical testing protocols and related documents,
  • Monitoring of clinical trials using e-CRF in various CROs in USA
  • Interaction with clinical research organization within L’Oreal (USA and France)
  • Available for travel, both within US and some travel to France
5

Senior Scientist Raw Materials Portfolio Management Resume Examples & Samples

  • Work as part of a global team to ensure the sustainability and security in use of our raw materials
  • Support and develop the business, by valuing and continuously improving the L’Oréal portfolio of raw materials used in formulations
  • Provide assistance to US laboratories in matters pertaining to raw materials used in L’Oréal formulations
  • Leads the securing of specific raw materials via dual sourcing approaches and diversification by coordinating activities of the lab, Purchasing, Quality, and DIMP, providing regular proper communications summarizing the activities, and making suggestions for next steps
  • Management of technical data in order to ensure data compliance with chemical and cosmetic regulations. Dossiers must be reviewed, evaluated for inconsistencies, and corrected as necessary
  • Comprehend and answer the technical requirements of a laboratories’ requests
  • Contribute to the valorizing raw materials by suggesting alternative raw materials to laboratories based upon technical, regulatory, and safety knowledge of raw materials, as well as hosting supplier workshops
6

Senior Scientist Resume Examples & Samples

  • Data analysis, Data mining and pathway analysis on large scale multi-omics data (microarray/proteomics/NGS/metabolomics…) with a view to biomarker discovery and validation
  • Participation in experimental design and implementation of new strategies for subsequent comprehensive interpretation of biological data
  • System integration of multi-OMICS data for active molecule discovery, biomarker development and biological target identification
  • Identify key trends, networks and patterns in data and integrate with Skin biology experts to generate hypotheses
  • Monitor emerging computational and data analysis technologies to accelerate program objectives
  • Working in a multi-disciplinary team with lab scientists and IT professionals to support active molecule and biological target discovery
7

Senior Scientist Imaging & Augmented Reality Resume Examples & Samples

  • Scout for new technologies in imaging, augmented reality, and computer vision for application in the beauty industry
  • Benchmark such technologies from competing vendors and universities, including study design, imaging laboratory work and image and numerical data analysis as needed
  • When strategic technologies are chosen, manage complex projects with team members from diverse backgrounds in research, product development, application design and development, IT, and marketing
8

Senior Scientist Ii Innovative Raw Materials Technology Scout Resume Examples & Samples

  • Responsible for identifying and supporting innovative raw materials and technologies which will deliver important new benefits for L’Oreal’s products
  • Identifying key suppliers and building and maintaining strong supplier relationships
  • Act as regional technical expert of Polymers and Silicones
  • Identify and seek out Innovative Raw Materials/Technologies and potential suppliers for all cosmetic field applications
  • Work with the International Pole Manager on the global strategy of the Polymers & Silicones
  • Serve as a technical expert of Polymers & Silicones to the local R&D team; this includes technical understanding as well as basic regulatory, safety, and industry related issues
  • Foster relations with key suppliers, and act as key technical L’Oreal contact to regional suppliers
  • Introduce novel raw materials to all Research labs within L’Oreal, and support the development and coding of these raw materials by interfacing with the suppliers, labs, and support functions
  • Approximately 10% travel
  • A senior professional who operates with minimal supervision and will initiate projects
9

Senior Scientist Resume Examples & Samples

  • Lead the technical development on the new polymers, especially the conversion technologies. Manage day to day technical interactions with the external partners and solve the technical problems
  • Assist in identification and evaluation of the next generation conversion technologies, and the 3G and 4G feedstock technologies for renewable sourced polymers
  • Provide Sr. subject matter expertise in polymer chemistry. Establish and manage relationship with network of strategic technology providers, research institutes and universities as external resources
  • Establishing packaging Material research Strategies & technology platforms
  • 10+ Years in chemical or polymer industry research, development and Commercialization
  • Industry Recognition as a leader of polymer chemistry
  • Track record of identifying and commercializing new materials or conversion technologies to solve business problems
  • Expert knowledge of polymer industry, suppliers and cost structures
  • Knowledge of chemical industry and polymer materials manufacturing, processing and supply chain
  • Experienced in managing R&D within a business environment and communication to non-technical senior managers
  • Demonstrated record of thought leaderships across international businesses, suppliers and supply chain
  • Experienced in managing external partnership relations, especially with new technology providers, research institutes and/or universities
  • Knowledge of life cycle assessment and circular economy
10

Senior Scientist Resume Examples & Samples

  • Apply clinical and research skills in designing and developing assessment solutions in both print and digital formats
  • Contribute substantially to the development of innovative, digital assessment solutions for educational psychology, mental health, neuropsychology, etc
  • Work with others to develop new digital assessment systems that combine scores from current testing tools to solve complex diagnostic and interpretive challenges for clinicians in practice
  • Contribute to the corporation's strategic planning
  • Disseminate knowledge, particularly the results of project related research through the publication of peer reviewed journal articles, technical reports, conference presentations, etc
  • Review other staff members' manuscripts for conference presentations, journal articles, and other Pearson publications, and maintain current knowledge of Pearson’s principal products and services
  • Consult on important clinical and research issues with all Pearson product development teams
  • Address issues related to the development, reliability, validity, interpretation, and use of scores on assessments in print and digital formats
  • Serve as an expert in major facets of the projects, and assist in the development of new product proposals in both print in digital formats
  • Contribute to ongoing processes to improve quality and efficiency of development activities (e.g. systems, processes, procedures)
  • Develop professional relationships as a representative, consultant, or advisor to external advisory and policy boards and councils, research organizations, educational and medical institutions, educators, and top management
  • Doctoral degree in psychology, neuropsychology, school psychology, education, communication disorders, or a related field with a solid quantitative background
  • Post-doctorate experience reflecting at least 10+ years of progressively responsible clinical research responsibilities in the area of assessment and / or treatment
  • Outstanding credentials and experience as both a scientist and practitioner
  • An extensive collection of research in peer reviewed journals, and presentations at professional conferences on issues relating to clinical assessment
  • Strong writing and speaking abilities, and effective interpersonal skills
  • A high level of technical competence in and demonstrated application of assessment, measurement, and research methodologies
  • Strong experience adapting standard cognitive tasks for digital presentation while preserving, or improving the construct measured by the original task
  • A commitment to promoting educational opportunity and human development
11

Senior Scientist Resume Examples & Samples

  • Develop and validate PCR-based molecular diagnostic assays using a variety of platforms
  • Present experimental data to small working groups as well as to the larger project teams. Present data in scientific meetings
  • Work in a dynamic matrix environment with high degree of independence. Actively cooperate and effectively communicate with other internal or external groups
  • Maintain impeccable records of raw data including notebooks and computer generated data files, quantitative analysis of data, laboratory protocols, and summary reports
  • M.S. or Ph.D. in biological or chemical sciences
  • Minimum of 5 years experience (with Master’s degree) or 2 years (with Ph.D) in academic or industry environment, preferably in the diagnostic industry
  • Experience with Molecular Biology areas including PCR, qPCR, DNA sequencing, nucleic acid purification, nucleic acid quantitation, and gel electrophoresis. Experience with and/or knowledge of high resolution DNA melt analysis a plus
  • Experience validating and transferring diagnostic assays to manufacturing is a plus
  • Strong analytical abilities required for design of experiments, data analysis, and reporting
12

Senior Scientist Human Computer Interaction Resume Examples & Samples

  • Demonstrate expertise in interface design and optimization to maximize user efficiency
  • Possess a strong understanding of state of the art UI design tools, methodologies and best practices
  • Be able to clearly articulate and implement technical requirements for desired UI functionality
  • Identify strategic partners in academia and industry to develop HCI capabilities
  • Hourly
  • Procurement
  • Strategic Planning
13

Senior Scientist Intelligent Systems Resume Examples & Samples

  • Act as principal investigator, leading multidisciplinary teams focuses on creative, integrated solutions for business and technical challenges
  • Be able to communicate openly and effectively to both technical peers and senior management
  • Government Relations
  • Human Resources
14

Senior Scientist Resume Examples & Samples

  • PhD with 0-2 years of experience
  • Master’s degree with 5+ years of experience; or
  • Bachelor’s degree with 10+ years of relevant experience
15

Senior Scientist Resume Examples & Samples

  • Bachelor’s degree required; Master’s degree preferred
  • 4+ years of PCR related research experience
  • Experience in blood screening and virology preferred
16

Senior Scientist Ii Manager Resume Examples & Samples

  • Lead, design, develop, and conduct and/or review experiments in order to deliver new products; evaluate ingredient, product or packaging safety, efficacy or claims; and play a leadership role in the initiation of product development projects with brand and new product marketing
  • Coordinate and manage product development resources to provide direction, supervision, focus and support to product development activities from initiation to completion. Play a leadership role in the initiation of projects, assigning of resources, prioritizing project loads and leveraging resources from appropriate company groups within the organization
  • Engage with NA Strategic Foodservice Customers to deliver new beverage choices
  • Provide technical leadership to represent R&D to all other departments, to act as scientific, regulatory, technical or quality expert and consultant and providing support to manufacturers, bottlers and customers
  • Utilize extensive knowledge and expertise to provide direction to new technologies and potential proprietary capabilities for the company in the area of juice and juice drinks, and health and wellness concepts
  • Project and process management skills
  • Presentation, verbal and written skills
  • Judgment and decision making skills
  • Strategic thinking, creativity and proactivity
  • Leadership and collaboration: exercises good general management disciplines
17

Senior Scientist Resume Examples & Samples

  • 55%
  • BS/MS in biology related field with 8+ years of industrial pharmaceutical experience in mammalian cell culture or PhD with post-doctoral/industrial experience (3-5 years), in vitro cell based assays, cell culture, immunoassays, electrophoresis, and immunoblot techniques required
  • Level and Title may be adjusted commensurate with experience
18

Senior Scientist Resume Examples & Samples

  • 60%
  • A Ph.D. in Life Sciences with emphasis on Biophysics, Physical Chemistry or Biochemistry is required
  • Five to ten years of combined postdoc/industry experience in macromolecules, especially in proteins and antibodies, is required
19

Senior Scientist Resume Examples & Samples

  • Designs, proposes, and leads the instrumental test plans for innovation projects and task forces related to hair styling & texture
  • Manages the hair styling and texture instrumental team member(s)
  • Evaluates and summarizes published literature (internal and external) on various topics surrounding hair and hair testing
  • Works on expanding hair knowledge, with particular focus on ethnic hair
  • Organizes, plans, and effectively executes instrumental testing to support aid to formulation and innovation studies for hair styling and texture projects
  • Maintains instrumentation and laboratory equipment and ensures proper operation/maintenance documentation
  • Analyzes instrumental test data and writes reports and memos to clearly communicate findings and share information with colleagues
  • Works on development of new methods and improvement of existing methods, and evaluates new equipment for use in innovation and aid to formulation testing
  • Maintains laboratory notebook in accordance with standard operating procedures; and
  • Develops ways to improve efficiency of daily operation of the Instrumental Evaluation group
20

Senior Scientist Mems Resume Examples & Samples

  • Develop rapid prototypes of concept products utilizing deep knowledge in electronics, sensors and optics
  • Contribute to the translation and strategic direction of clinical projects (monitoring of cross-functional projects with other entities of R&I, active participation in project meetings and reporting)
  • Coordinate projects between L’Oréal laboratories and external collaborators
  • Demonstrate creativity and resourcefulness in proactively identifying and proposing solutions to issues that may arise during the course of a research project
  • Approximately 20 - 40% travel
21

Senior Scientist Resume Examples & Samples

  • Work on difficult engineering tasks with little to no supervision, yet assuring good coordination with team members and leader for attaining the project goals
  • Be a good team player
  • Act as task leader or principal investigator, leading multidisciplinary teams focused on creative, integrated solutions for business and technical challenges
  • Author technical papers and reports including publications in top journals and conferences; be active in related technical communities
  • Communications
  • Engineering
  • Internal Audit
  • Project Manager
  • Research/Development
22

IBS Young Scientist & IBS Senior Scientist Program in Resume Examples & Samples

  • Schedule for 2015
  • “FAQ: IBS YS·SS Programs”
  • Introduction
23

Senior Scientist Resume Examples & Samples

  • Responsible for providing leadership in translational biomarker strategies and execution plans and delivering scientifically-driven biomarkers to support different stages of drug development programs across Shire portfolios
  • Liaise with discovery biologists, bioanalytical scientists, non-clinical and clinical teams, as well as external collaborators to set biomarker goals/expectations and implement innovative techniques to identify and validate biomarkers of different purposes (e.g., target engagement, mechanism of drug action, pharmacodynamics, proof of concept, etc)
  • Responsible for designing, implementing and managing a wide range of bioanalytical and biomarker assay development, validation, sample analysis, and reporting in accordance with appropriate regulatory compliances
  • Broad experience in discovery and development of pharmacogenomic and other biomarker entities using mRNA Next Generation Sequencing, mass spectrometry-based global and targeted profiling, as well as ligand-binding assays
  • Experience with regulated bioanalysis of gene therapeutics, such as RT-PCR etc
  • 50% Design biomarker strategy and implement high complexity bioanalytical assays
  • 20% Manage external vendors/CROs to meet sample testing timelines
  • 10% Performs high-level review of assay results/interpretation/reports to ensure technical
  • Ph.D. degree in molecular and cellular biology or related disciplines with a minimum of 3-6 years industry experience in translational biomarker research and assay development
  • More experienced candidate may be considered for Principal Scientist position
  • In-depth understanding of drug development processes and associated biomarker requirements
  • Broad experience in fit-for-purpose biomarker assay development for various molecular entities (small molecules, proteins, and DNAs)
  • Prior experience in biomedical application of mass spectrometry is favored
  • Experience in pharmacogenomics such as mRNA profiling and large data analysis for biomarker, target, disease pathway, or drug mechanism of action studies is a plus
  • Familiarity and experience with global regulatory guidelines, expectations and corresponding industry best practices is preferred
  • Prior experience managing CROs
  • Recognized scientific leadership as documented by track records of publications and external presentations
  • Strong problem-solving, presentation, and communication skills and the ability to work in a fast-paced and dynamic team environment
24

Senior Scientist Resume Examples & Samples

  • Lead activities associated with their area of expertise. This includes but is not limited to
  • Act as scientific, regulatory, technical or quality expert and consultant by responding to targeted questions from the field or other departments/business units and providing support to bottlers, and customers. This includes acting as a consultant for other technical personnel in the Company
  • In consultation with Global Quality and other laboratories, identify and/or develop test methodologies for testing. Includes review of literature, method validation / transfer etc
  • Work with other Global test facilities to ensure collaborative sharing of ideas and experiences. As an SME, coordinate SME teams in given area of expertise and be responsible for driving improvement across multiple geographies
  • Coordinate with various functions within TCCC on different projects/programs, including, science, standard and methods teams, PICASSO project team, etc
  • Perform advanced complex analysis of ingredients, beverages and finished product using high end analytical instrumentation including GCMS, LCMSMS etc
  • Provide SME support to method validation. Conduct validation in accordance with predetermined global guidelines
  • Conduct research into new methodologies and techniques to support both internal processes as well as external needs (eg bottlers)
  • Act as SME for EQC in scientific discussions centred on analytical interpretation of test results. Readily converts complex data and information into simple to understand facts and opportunities
  • Works with Managers within EQC to develop internal talent for future growth
  • Chromatography (LC) with UV/Vis, PDA, RI, Fluorescence, MS/MS Triple Quad, and MS-TOF detection
  • Foundational knowledge of chemistries related to one or more of the following areas: pesticides, volatile, semi volatiles, metals, microbiological analysis
  • Exposure to analytical programs related to carbonated / sensitive beverages highly desirable
  • Certified in accordance with a Global Analytical or regulatory Organization such as AOAC, JECFA, WHO, EFSA
  • Knowledge of SPC, GLP, food safety, ISO17025
  • Analytical skills, computer skills-data analysis, LIMS
  • Minimum of 12 years analytical working experience in the food, pharmaceutical or similar industry. At least 5 years of experience in a leadership or SME role associated with the operating of a department using advanced analytical techniques
  • Extensive experience in flavour chemistry from a reputable flavour house or industry that deals with or uses flavours
  • Experience managing technical relationships with external customers in a third party lab environment
  • Publications in reputed scientific journals
  • Knowledge of advanced analytical instrumentation and EU regulations
  • Required language skills: Proficiency in French or Dutch and English
25

Senior Scientist Resume Examples & Samples

  • This individual should possess the ability to speak the language of Big Data by leveraging insights from multiple data sources (Social, Technological, Economic, Environmental and Political forces) to help connect facts that will drive future innovation for that region
  • Demonstrate the ability to leverage exploratory research to tap into consumers at a much deeper level and quantify those learnings for action
  • Exhibit a curiosity for people and what motivates their behavior and the ability to link those insight to business and technology
  • Good communication skills including ability to write concise, informative reports and verbally present complex technical information and unarticulated consumer needs to non-technical audiences. Ability to listen and identify project objective and influence research plan
  • Must be an effective influence manager capable of getting the clients and/or business to do the right research at the right time thereby increasing the client’s success rate
  • Must be proficient at working with numbers from surveys and data in the form of statistics
  • Possess the skills necessary to look beyond the obvious to see how data and facts can be linked together to create more meaningful conclusions
  • Proficientknowledge in the area of quantitative research which involves the design and implementation of quantitative sensory and consumer research studies, including creation of the research design, implementation and data gathering, data analysis, and trend analysis, interpretation, implications and next steps
  • Sound knowledgeof product development and the R&D process associated with the food and beverage industry
  • Demonstrates proficiency in technical risk assessment used to identify, evaluate and mitigate project risks with a strong working knowledge of franchise and opportunity risk profiles
  • Demonstrates proficiency in the use of experimental designs (including two-level factorials and optimization strategies), data management, qualitative research techniques and research-on-research applications
  • Demonstrates proficiency in the process of leading others as a result of expertise in specific area of discipline. This includes serving as a technical mentor and resources for others
  • Sound knowledge of sensory and consumer testing techniques and principles including a deep understanding of descriptive analysis (DA) and the relationship to consumer data to identify sensory drivers of consumer liking
  • Working knowledge of statistics including the appropriate use of statistical techniques to analyze and interpret data (including parametric and non-parametric methods, ANOVA, and modeling tools) and the design of experiments (DOE)
26

Senior Scientist Resume Examples & Samples

  • Highly motivated biologist to perform in-vitro and potentially in-vivo laboratory experiments primarily related to Hematology-Oncology programs within Discovery Biology and Translational Research
  • Knowledge of a diverse range of cellular experiments to measure changes in cellular activity in support of in-vitro and in-vivo studies is required
  • Experience in the use of biologics is a plus. Prior experience with PDX models, SCID-hu models 5TMM models is ideal. Experience with isolation, purification and quantification of bone-marrow derived cells for estimating tumor burden, efficacy of therapeutic and biomarker screening is a plus
  • Employee will establish experimental approaches, under general supervision, addressing mechanism of action of drug candidates such as cellular signaling, uptake and kinetics, localization and recycling of drug product within target cells. In addition, employee will be expected to develop pharmacodynamic markers, with direct supervision, to incorporate into the early development of drug candidates
  • Familiarity with handling small rodent models, in vivo experiments on models of human disease is a plus
  • Employee will interact with scientific personnel from other departments, as well as with external vendors
  • Expected to prepare scientific reports, participate in team-wide scientific presentations
  • 55% Primary function is to work as dedicated experimental resource for hematological oncology projects. Perform experiments to develop in-vitro and cell based assays to validate targets and test MoA of therapeutics,validate up to in-vivo animal models
  • 15% Analyze, interpret and summarize data; prepare data for presentation and reports
  • 10% Analyze, interpret and summarize data; prepare data for presentation and reports
  • 10% Manage external vendors required to deliver on project goals
  • 10% Participate in due diligence activities
27

Senior Scientist Resume Examples & Samples

  • 60% - Experimental design and execution
  • 15% - Manage internal and external resource for protein and cell line generation
  • 15% - Perform background research of biomolecules, participate in project teams, and provide strategies for trouble shooting for colleagues
  • 10% - Composing scientific presentations, writing research reports and contribute to patent filing and external publication
28

Senior Scientist / Scientist Resume Examples & Samples

  • Design and conduct experiments required to advance projects
  • Perform hands-on molecular biology engineering, production and characterization of research scale viral vectors. Establish existing or develop new vector characterization assays
  • 20%
  • Communicate with members of Discovery Therapeutics, Discovery Biology and Non-Clinical Development and Pharmaceutical Development
  • PhD in virology, genetics, pharmacology or related biological science and strong track record of scientific publications is required
  • Experience in viral vector knowledge is required. Experience working with adeno-associated viral vector is a plus
  • Hands on experience and proficiency with molecular biology including in silico vector design, DNA cloning, capability in designing gene expression vector constructs, performing transient and stable transfection in mammalian cells
  • Hands on experience with research scale vector production and purification. Experienced in using column-based purification method and trouble-shooting is required
  • Hands on experience and proficiency with the use of various analytical techniques including but not limited to PCR, qPCR, RT-PCR, ELISA, MSD, Western, Silver-stain, reporter-gene assays, enzymatic assays, cell-based assays, nucleotide hybridization techniques and flow cytometry
  • Ability to design and perform experiments for assay development and troubleshoot assay development with minimum supervision. Experiment in in vitro and in vivo experimental design and execution in individual and team settings
  • Data-driven, critical thinking, analytical and ability to interpret results and present the implications to manager and teams
  • Good organizational skills, and attention to detail, are essential
  • Excellent interpersonal, written and oral communication and presentation skills
  • Must be open to the ideas of others and utilize different perspectives to drive towards creative solutions in a timely manner while maintaining the highest of scientific and ethical standards
  • Ability to establish and develop relationships with internal cross-discipline scientists
  • Exhibit knowledge and sound judgment of interpreting experimental results
  • Highly independent and motivated to adapt to new environment; has ability to adapt to a fast paced environment and deliver results with a team-working spirit
  • Expected to work independently with modest supervision, demonstrate motivation in pursuing scientific answers
  • Independently develop solutions to diverse problems, including identifying methods for experimental design which may require sophisticated planning and cross-functional collaboration
  • Expected to be accountable for effectiveness and timelines of completion of milestones and project goals
29

Senior Scientist Resume Examples & Samples

  • Develop novel hair products with identified raw materials and technology by designing the formula around materials to fully explore the potential benefits of the raw materials and technology
  • Work closely with Innovative Raw Materials Department and suppliers to identify new raw materials and new technology with potential benefits for cosmetic applications
  • Put in place a patent strategy that will safeguard the formula and technology invented
  • Work closely with Hair development lab to ensure smooth transition of new products and technologies
  • Communicate and present the technology and new products to senior management and colleagues at different geographic locations and different categories within the company
  • Maintain good knowledge of competitor’s patent environments and close awareness of consumer need gap and marketing trends
  • Preferably with 1-2 years of postgraduate experience
  • Be able to work under pressure and handle multiple projects simultaneously. Be able to work independently and to drive the project forward with high efficiency
  • Creative and self-motivated. Be able to think out of the box and willing to take an extra step to get job done. Excellent communication and presentation skills
  • Foreign language skills in French a plus
30

Senior Scientist Clinical Pharmacogenetics Resume Examples & Samples

  • Leading strategic pharmacogenetic approaches to enable drug development decision making
  • Analysis and interpretation of pharmacogenetic data
  • Emphasis on interpretation of results from genome-wide association studies (GWAS) data as it pertains to clinical development strategy and causal human biology
  • Informatic analysis of data sets to inform further experimental design The role sits at the critical interface between statistical analysis, pre-clinical and clinical drug development. The successful candidate will be expected to work with biologists, geneticists, clinicians and statisticians to develop strategies, perform data analysis and interpretation in the context of drug development programs. Given the multi-disciplinary nature of the position, very strong collaboration and communication skills are required. A deep understanding of genetics, pharmacogenetics and informatic processing of genetic data is required
  • Working closely with clinical drug development teams, biologists, and statisticians to design genetic studies, including writing and defending project approval documents
  • Interpretation of ADME genetic variation as it relates to PK and other clinical endpoints
  • Analyzing and interpreting large-scale pharmacogenetic data sets, including next-generation sequencing and GWAS data
  • Identify variants associated with human phenotypes and interrogate human causal biology. Follow up and interpretation of published data relevant to clinical programs that influence pharmacogenetic approaches and strategies
  • Written and verbal communication of study results to project teams, including proposals for further experiments to validate key findings and completing regulatory reports
  • Collaboration with other geneticists for target identification projects, using clinical data and biological validation of GWAS results
  • Manage a portfolio of projects to review and prioritize new and on-going projects
  • Deep understanding of human genetics is required, including experience understanding the role of pharmacogenetic variation to clinical phenotypes of medical relevance
  • Extensive experience in the genetics and function of ADME genes and their role in relationship to pharmacokinetics and other clinical endpoints
  • Knowledge in the design and bioinformatics analysis of large-scale human genetic datasets, array based and next-generation sequencing data
  • Experience in interpreting GWAS data, including concepts related to population genetics (e.g., linkage disequilibrium, genetic architecture of human disease) and functional annotation of human genetic variation (e.g., coding and non-coding variants)
  • Strong communication, collaboration, and leadership skills, including an ability to communicate complex data analysis results in a clear, concise manner to biologists, clinicians, and senior management
31

Senior Scientist Resume Examples & Samples

  • Coordinate and execute strategic projects in the area of connected devices for the consumer electronics sector
  • Support business development activities, including assessing technologies developed in other organizations such as university labs and start-up companies
  • Interface with business development, contract, and patent attorneys to execute contracts and patents
  • Approximately 20 - 30% travel
32

Senior Scientist Resume Examples & Samples

  • 25%
  • Good knowledge and experience to apply Quality by Design principles and statistical analysis tools to evaluate drug product process and manufacturing process
  • Must be well-organized and self-disciplined
  • Must be able to multi-task in a timeline-driven and dynamic team environment while providing quality work
  • Strong interpersonal skills with the ability to interact effectively and appropriately within and cross functional lines
  • Demonstrated sound technical writing skills
  • Customer focused, results oriented, science driven and embrace Shire’s values
33

Senior Scientist Resume Examples & Samples

  • 8+ years of experience in the Pharmaceutical industry
  • Master's Degree in Natural Science
  • Proven skills in pre-formulation, dosage form design and/or analytical method development
  • Proven scientific skill and ability to do independent scientific work with no guidance
  • Proven skills in QbD and Experimental design
  • Solid analytical skills
  • Great interpersonal skills
  • Ph.D
  • Experience in the pharmaceutical GXP regulated work
34

Senior Scientist Resume Examples & Samples

  • Development of assays for the characterization of different classes of enzymes
  • Determination of kinetic parameters KM, Vmax and kcat and optimal working conditions for cellulosic enzymes
  • Development and optimization of enzyme cocktails for the degradation of different biomasses
  • Preparation of memos and reports to management
  • Management of designated projects, coaching and supervision of junior staff to meet strict deadlines
  • Acquire and maintain theoretical and practical knowledge of enzymatic hydrolysis applications, commercial markets for enzymes and competing products
35

Senior Scientist Resume Examples & Samples

  • Design, develop, conduct and/or review experiments (e.g., laboratory or process experiments) in order to deliver new products; evaluate ingredient, product or packaging safety, efficacy or claims; or evaluate new ingredients, materials, products or processes. Act as scientific, regulatory, technical or quality expert and consultant by responding to targeted questions from the field or other departments/ business units and providing support to branches, bottlers and customers. This includes acting as a resource for general information and acting as a consultant for other technical personnel in the Company
  • Access and utilize internal/external relationships to deliver science, technology and product innovation, and to support ingredient supply. Provide food science and beverage technology support and consultancy to other departments within the organization
  • Record data from analyses or experiments in a computer, log book or laboratory notebook
  • Strong technical fundamentals and problem solving ability
  • Cross functional and project management skills
  • Experience in juice, liquid food product development and commercialization a plus
  • Previous experience presenting to external customers a plus
  • Intellectual Property: Knowledge of securing intellectual property rights through patents, negotiations with technology owners, securing competitive agreements and maintaining confidentiality
  • Basic Project Management: Knowledge of project management principles and the ability to apply the principles, tools and techniques to develop/plan, manage or execute projects or work-plans to ensure successful completion (e.g., on time, within budget)
  • Building Technical Relationships: Ability to apply technical knowledge and establish credibility with highly technical audiences in order to build technical relationships that will benefit customers or the Company
36

Senior Scientist Resume Examples & Samples

  • Initiate, direct and execute all pre-clinical scientific research and/or development strategies in research and/or development
  • Investigate the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problems
  • May participate in development of patent applications
  • Interface with various departments and serves as internal consultant
  • Education Required: MS. or Ph.D. in a biological or chemical science or engineering degree
  • Experience Required: Minimum 6 years of experience in scientific research and development, with 3+ years of experience in an industry setting preferred
37

Senior Scientist Resume Examples & Samples

  • Responsible for analytical method development and validation of cGMP compliant and state of the art methods
  • Develops and executes protocols for test method validation/transfer and equipment qualification
  • Ensures timely and right first time method transfer to/from CoE to Quality Laboratories, including the issue of protocols and reports
  • Maintains a current understanding of regulations as applied to laboratories
  • Conducts laboratory investigations as necessary and issues the corresponding reports
  • Responsible for development, writing and updating of standard operating procedures
  • Troubleshoots analytical methods as needed to ensure proper functionality
  • Responsible for assuring adherence to local and national regulations, cGMP's, SOP's, company policies and procedures
  • Authors technical reports and regulatory supporting documents, as necessary
  • Keeps abreast of relevant new technologies / capabilities and regulatory initiatives / requirements
  • Responsible for calibration and maintenance of analytical equipment
  • Experienced with laboratory instrument qualification and troubleshooting
  • Experienced in laboratory GMPs in pharmaceutical or medical device industry; Combination product familiarity preferred
  • Experienced in cleaning validation
38

Senior Scientist, Cell Based Discovery Resume Examples & Samples

  • Serve as a global subject matter expert for Cell-based Discovery Technologies
  • Deliver innovative, cutting-edge technologies for sweetener and ingredient discovery
  • Communicate effectively to peers and management on technical approaches and risk
  • As a global thought-leader, must build internal and external credibility and relationships
  • 5-10 years of research training/business experience beyond PhD
39

Senior Scientist, Application Research Resume Examples & Samples

  • Develop new sweetener rapid evaluation and characterization tools and processes that can effectively support / feedback the new sweetener technology development
  • Identify and work with internal and external technical resources to build fundamental understanding of the impact of high intensity sweetener on associated beverage attributes, i.e. taste profile etc
  • Lead the development of new sweetener system optimization tools and processes that maximize the new sweetener performance in different product matrix, which will be basis for new sweetener commercialization
  • As sweetener application expert, provide consultant, technical support to new product development teams to enable the smooth commercialization of new sweeteners
  • Support Prototype production as needed (thought leadership and execution)
  • PHD on related fields – food science, organic chemistry etc
  • 5+ years of food ingredients / flavor research experiences in food and beverage industry
  • Proven track record of successful new ingredients / flavor research and application development, experiences on beverage product development is a plus
40

Senior Scientist Resume Examples & Samples

  • Fundamental MD simulation knowledge and experience
  • Experience with material properties prediction (Tg, isotropic phase structure, moduli, diffusion behavior of small molecules, polymer/polymer interaction, etc.)
  • Experience in protein/ligand binding thermodynamics and docking simulations; homology structure and similarity analysis for protein and enzyme systems
  • Experience in chemo informatics and general 2D modeling
  • Strong statistical background in linear, non-linear statistical methods, network learning algorithms etc
  • Experience in some programming such as in Matlab, Python, Java, C++, or equivalent
  • Strong experience in Ab initio methods for thermodynamic and kinetic screening of chemical systems
  • Strong breadth of knowledge in IP. Build the IP Strategy and establish a strong IP portfolio, building, filing patents, publications, and technical implementations
  • Well versed in the literature of what’s out there and able to perform literature analysis
  • Methodology selection and results delivery – knowledge of different method for simulation. Must be able to work with collaborators to understand the current needs and priorities and deliver the right combination of speed, simulation scale, and results accuracy
  • Simulations Development – Be able to develop and standardize certain methods for use and application by the larger technical community. Must be able to train and teach the technical community on how and when to use certain tools as well as the boundaries in which the results are applicable
  • Documentation and Communication and Project Management – Demonstrate ability to provide a high level of traceable and consistent documentation of all simulation activities. Must be able to communicate objectives, effort loading, and results to a large mix of technical and non-technical audiences. Must be able to communicate and document results and connections to business plans and project objectives. Must be able to work with CROs and consultants to accelerate project work or access capabilities that are not available at TCCC
41

Senior Scientist Resume Examples & Samples

  • Serve as the TCCC global subject matter expert for Ag-based technologies featuring accelerated plant breeding, agronomy, and sustainable crop development
  • Recommend and deliver innovative, cutting-edge technologies and partnerships to accelerate the cost-effective supply of ag-based production of key commodity and non-commodity ingredients and packaging material feedstocks
  • 5- 10 years of relevant research training/business experience beyond PhD
42

Senior Scientist Drug Product Mfg Sci & Tech Resume Examples & Samples

  • 25% Lead and execute drug product related activities to achieve the project goals
  • 25% Perform data analysis for continuous process improvements and life cycle initiatives, aimed at improving drug product manufacturing process robustness and consistency. Provide technical expertise and leadership in proactively identifying and addressing drug product development gaps to improve manufacturing process through life-cycle management
  • 15% Provide technical support for deviations, change controls, CAPA and GMP investigations for Shire biologics commercial drug products
  • 15% Provide technical support for regulatory submissions, responses and inspections
  • 10% Serve as a drug product representative to provide sound technical and scientific leadership and support within cross functional project teams including CMC, quality investigation and process improvement
  • 10% Provide support for departmental operations to improve the existing system(s) and processes, and evaluation of new technology and contract partner(s)
43

Senior Scientist, Microbiology Resume Examples & Samples

  • Provide the framework and tools for ensuring the quality and integrity of products through the on-going development and refining of The Coca-Cola Operating Requirements (KORE)
  • Provide appropriate technical support for microbiological inquiries and concerns to product developers, process engineers, and business units. Provide guidance on microbiological sensitivity of ingredients, processes, and finished products
  • Collaborate with external laboratories, research institutions, and universities to address research and troubleshooting needs. Coordinate and conduct microbiological examination of ingredients and finished products, internally or externally, to determine their microbial load and sensitivity
  • Support Microbiological and Laboratory quality standards, specifications, requirements and methods (e.g., concentrate/beverage base, ingredients, packaging, beverage, processes, and new technology) following the KORE process in order to ensure quality and integrity of products, and to protect the trademarks of the Coca-Cola Company
  • Determine training needs, tools and communication aids to provide training to R&D partners
  • Review and recommend changes to proposed formulas, products or packages to ensure effective and efficient production including an evaluation and review of thermal processing parameters of a formula prior to approval. Work closely with Global R&D microbiology team to support the use of the Microbiology Decision Tree and the exception process
  • Review and evaluate reported incidents and crisis (i.e., highly-urgent product related problem with immediate negative implications for the Company) and formulate a plan of action for handling the incident/issues based on area of expertise/responsibility (IMCR)
  • Lead the Shanghai Microbiology Team, building the right capability and expertise to support short and long term R&D strategies and initiatives. Support the development of a high performing Global R&D Microbiology group
  • Participate in or provide expertise to external organizations/committees/boards such as scientific or industry groups to represent the Company or customers and influence outcomes
  • Advanced Food Microbiology: Ability to understand and interpret advanced microbiological studies as they apply to food and water safety. Ability to understand diseases caused by food and water contamination and design strategies to address issues related to these diseases. Includes awareness of new pathogens that may affect company products and the ability to propose and introduce new assays. Knowledge of food and water microbiology used to make judgments about the safety of ingredients, beverages, manufacturing techniques, packaging and storage conditions
  • Setting Standards & Specifications: The ability to set and maintain standards and specifications using knowledge of ingredients, packaging, beverage production and/or concentrate manufacturing. This includes reviewing or approving requests from customers for changes to established procedures
  • Laboratory Practices: Knowledge and application of Good Laboratory Practice (e.g., handling of chemicals and glassware, preparation of standards and reagents, proper measuring techniques, data management, housekeeping)
  • Food Science: Knowledge of principles and techniques of basic food science and their application to the beverage and food industry
  • Manufacturing Processes: Knowledge of basic manufacturing and assembly processes; includes understanding how design changes will affect these processes with regards to lead time, resource requirements, acquisition cost and tooling cost. Knowledge of material handling processes for moving materials/products throughout the manufacturing and distribution process
  • Research Expertise: Use of sound, science-based methods and cooperative interpersonal style to help build cohesive local and global teams. Possess the ability to apply principles, tools and techniques to develop research protocols, and to manage and conduct trials and studies on a timely and financially manner
44

Senior Scientist, Application Research Resume Examples & Samples

  • Develop new ingredient rapid evaluation and characterization tools and processes that can effectively support / feedback the new ingredient technology development
  • Identify and work with internal and external technical resources to build fundamental understanding of the impact of ingredient on associated beverage attributes, i.e. taste profile etc
  • Lead the development of new ingredient system optimization tools and processes that maximize the new ingredient performance in different product matrix, which will be basis for new ingredient commercialization
  • As ingredient application expert, provide consultant, technical support to new product development teams to enable the smooth commercialization of new ingredient
45

Senior Scientist Resume Examples & Samples

  • Ingredient, Flavor and Beverage development
  • Preparation, management and protection of proprietary formula composition and technical information
  • Product commercialization knowledge
  • Independently lead multi-disciplinary projects
  • Collaboration with internal Business partners and external suppliers
  • Research and evaluate new developments or trends in beverage-related industries
  • Guide daily activities of Associate Food Scientist
46

Senior Scientist of Basic Science Research Resume Examples & Samples

  • Ensure resources and equipments kept in good working conditions
  • Provides data analysis and interpretation, and assesses impact of the data on the project
  • Designs and or conducts experimental strategies with general guidance from supervisor, assist the BSR scientist to do basic research
  • Understand skin knowledge and consumer needs to help developing new products
  • Literature search to explore new direction of our study in the future
  • Work efficiently in a collaborative team environment
  • Master degree in cellular biology, molecular biology, medicine or a related field
  • Have experience in cell culture and basic molecular biological experiments
  • Understand basic statistical analysis method
  • Fluent written and verbal skills in English
  • Skilled in Microsoft Office softwares
  • Quick learner, independent and innovative thinking, strong responsibility, self-motivated and cooperative
  • Be interested in cosmetics research and development and willing to grow with the company
47

Senior Scientist Resume Examples & Samples

  • 60% Planning and performing scientific experiments
  • 20% Train fellow scientists with analytical techniques, explore new technologies for analytical characterization
  • 10% Communicate with supervisor and fellow scientists regarding experimental design and results
  • 10% Prepare research reports and summary
48

Senior Scientist, Organic Chemistry Resume Examples & Samples

  • Strong technical background in Organic Chemistry including natural products chemistry/complex carbohydrate chemistry/protein chemistry/lipid chemistry as evidenced by proven track record including publications and patents
  • Strong technical expertise in discovery of bioactives using structure-activity relationship
  • Strong background to functionalize and characterize these ingredients including synthesis, purification and structure elucidation of biologically interesting compounds using a variety of chromatography and spectroscopic techniques
  • Requires ability to collaborate externally and internally with global Research & Innovation scientists
  • The candidate must be able to work independently and has excellent written and oral communication skills
  • Leads peers, scientifically, by combining sound judgment, strong initiative and thorough methodology
49

Senior Scientist Resume Examples & Samples

  • Proficient knowledge in the area of quantitative research which involves the design and implementation of sensory and consumer research studies, including creation of the research design, implementation and data gathering, data analysis, interpretation, implications and next steps
  • Demonstrates proficiency in technical risk assessment used to identify, evaluate and mitigate project risks with a strong working knowledge of franchise and opportunity risks
  • Demonstrates strong working knowledge in the use of experimental designs (including two-level factorials and optimization strategies), data management, qualitative research techniques and research-on-research applications
  • Working knowledge of psychophysical measurement methods (both theory and application)
  • Competent to innovate or modify methodologies for product or ingredient evaluation according to business requirements
  • Working knowledge of sensory assessment of food/beverage ingredients and sweeteners
  • Experience with automated sensory data collection systems
  • Must be an effective influence manager capable of getting the clients to do the right research at the right time thereby increasing the client’s success rate
  • Typically organizes and prioritizes work but must occasionally request exceptions to established procedures
  • Establishes goals and policies for areas of responsibility subject to review by top division executive. There is broad latitude for decision making
50

Senior Scientist Resume Examples & Samples

  • We are looking for people with varied experience with demonstrated ability to apply Text Mining
  • Candidates should hold an PhD or Masters (with relevant experience) in Computer Science, with
  • The candidate should have a demonstrated strong foundation in Machine Learning Theory with a
  • Prior experience working with very large datasets using Big Data tools and platforms (Hadoop, Pig, HIVE) is highly desirable
  • Experience in working with large text datasets
51

Senior Scientist R&D Resume Examples & Samples

  • Develop new technologies and demonstrate them in relevant environments. Advance the state of the art in cognitive systems technologies and related applications, as a contributing member of teams led by others or as team leader
  • Develop algorithms and software to prototype solutions and evaluate new concepts
  • Develop new ideas for both external and internal projects
  • Provide technical support to the pursuit of government funding opportunities for leading-edge research in cognitive systems. Key areas of interest include remotely piloted flight, autonomous systems, and research in underlying technologies, for example, integration of symbolic and connectionist approaches and natural language interfaces
  • Participate in the broader research community, for instance through collaboration with other internal and external research organizations and participation in industry forums
  • Understand new technology trends, uncover non-obvious opportunities for Honeywell to provide value through new technologies, and help provide technology differentiation for Honeywell products
  • Execute internally and externally funded advanced technology projects successfully
  • MS or PhD in Electrical Engineering, Computer Science, Computer Engineering, Systems Engineering, Human Machine Interaction, or related fields
  • Experience in an R&D or advanced technology environment – two plus years for PhDs; four years for MS degree holders
  • Two plus years of recent experience in hands-on algorithm design and software development to evaluate new concepts
  • PhD in one of the fields mentioned above
  • Background in cognitive computing and associated tools in areas such as knowledge representation, reasoning, machine learning, planning, intelligent agents and natural language interfaces
  • Recent track record of leading new technology development programs as Principal Investigator
  • Recent track record of leading or contributing to winning proposals to government funding agencies such as DARPA, IARPA, NASA, AFRL and ONR
  • Background and interest in aviation and human-machine systems
  • Strong and active network of professional relationships
  • Experience in working with collaborators from academia and industry on leading edge research and technology development
  • Experience in the aerospace industry
  • Excellent skills in interpersonal communication and influencing stakeholders
52

Senior Scientist Resume Examples & Samples

  • Partnering with global and regional business cross-functional teams
  • Leading complex projects to deliver new and improved tissue and wipes products
  • Leading multiple projects having small work teams
  • A Bachelor’s or advanced degree in a related major scientific field or engineering discipline from an accredited college or university with a minimum of 8-12 years of experience in a variety of technical assignments
  • Experience in global product development
  • Ability to build and foster global relationships
  • Extensive project management experience - preferably with global projects
  • Demonstrated ability to work independently or as part of a team to complete projects within required time frames
  • A track record of strong project leadership capabilities
  • Demonstrated ability to translate consumer insights into feasible solutions including concept and prototype validation with end users
  • Demonstrated ability to solve complex business challenges
  • Experience working cross-functionally with business unit marketing on a global basis
53

Senior Scientist Resume Examples & Samples

  • A minimum of a Bachelor's degree and 5 years of analytical chemistry experience is required
  • A focused degree in Chemistry or Pharmaceutical Chemistry is preferred
  • Experiences in the pharmaceutical, consumer product, and/or chemical industries are required
  • A strong background in analytical instrumentation and method development using HPLC, UPLC, and GC is required
  • It is preferred that this candidate have experience performing instrumental and wet chemistry testing including FT-IR, UV-VIS, LC-MS, dissolution, titration, and other chemical analyses successfully
  • Familiarity with GMP’s is required
  • It is required that this candidate have strong technical writing skills and strong communication skills
  • This candidate will be able to handle multiple, competing priorities and work with minimal supervision to accomplish technical tasks
  • This position will be based within Fort Washington, PA and requires up to 10% domestic and international travel.R&D
54

Senior Scientist, Chemist Resume Examples & Samples

  • Advanced degree in Chemistry, Organic Chemistry, Biochemistry or related discipline is required
  • A minimum of 4 years of experience in related industries in an R&D setting is required
  • Strong knowledge in organic chemistry, .surfactants, detergents, disinfectants, sterilants, sterilization technologies, sterility assurance is required
  • A strong knowledge in biofilms, disinfectants efficacy test methods is preferred
  • Must have a strong knowledge in formulation development
  • A strong knowledge in analytical device (HPLC, GC, UV, etc.) is preferred
  • A strong knowledge in statistical analysis such as mixture design, DOE, optimization is preferred
  • Must be able to provide direction to assign staff on performing duties and ensure understanding of and compliance with applicable laboratory and safety procedures
  • A strong working knowledge of QSR, FDA / ISO guidelines is preferred.R&D
55

Senior Scientist Resume Examples & Samples

  • Support Quality Supervisor Labs in the initiation, design and prioritization of analytical projects
  • Support Quality Supervisor Labs in the preparation, review and approval of analytical protocols and reports
  • Support Quality Supervisor Labs in the selection and approval of chemical raw materials
  • Support Quality Supervisor Labs in the co-ordination, review and approval of laboratory investigations
  • Support Quality Supervisor Labs in the preparation and maintenance of chemistry methods, specifications and SOP’s in compliance with pharmacopoeial and regulatory requirements
  • Selection of contract laboratories, co-ordination of testing requirements and review of reports received
  • Ensuring GMP/GLP compliance in all aspects of the laboratory functions
  • Support Quality Supervisor Labs in the implementing a creative approach to improving accuracy, reliability and productivity within laboratory area group
  • Working effectively to troubleshoot and solve problems
  • Implementing appropriate safety procedures in the laboratory
  • Performing environmental and safety assessments for new chemicals
  • Ensuring compliance with chemical regulatory requirements, e.g. REACH Directive
  • Ensuring effective interaction and involvement with other departments and management
  • Third Level Degree
  • Minimum of 5 years experience in the medical device/pharmaceutical industry
  • Proven record in method development transfer and validation
  • A strong theoretical and practical knowledge of HPLC’s
  • Very good interpersonal, communication and presentation skills, along with an ability to deliver on targets and deadlines
  • Proficient in the use of MS Office and Chromatography systems softwareQuality (Generalist)
56

Senior Scientist, Computational Biology, Jhmi Resume Examples & Samples

  • Provide research direction and project leadership, develop innovative concepts for further exploration, and implement solutions that extend the state of the art
  • Design, develop, and operate computational pipelines for analyzing internal, external -omic data, and biomedical data to develop novel therapeutics and biomarkers
  • Implement bioinformatics tools for use by a broad community of scientists
  • Collaborate with an interdisciplinary JHMI team and across the Janssen therapeutic areas when appropriate
  • Maintain expert knowledge of computational tools and datasets in the microbiome field
  • Keep abreast of scientific literature, emerging approaches and innovations in the microbiome
  • PhD in Bioinformatics, Biostatistics, Computational Biology or similar field is required
  • At least 2 years leading interdisciplinary teams (e.g. of computer scientists, computational biologists, molecular biologists, and microbial ecologists) is required
  • Solid understanding of statistics, data mining, and visualization of biological data types is required
  • Experience working with large scale genomic data (e.g. gene expression, SNP, microarrays, etc) is required
  • Capable of developing strong influential relationships with scientific peers and stakeholders
  • Ability to work in interactive team environments while also conducting self-directed research within broader goals set by JHMI
  • Must be organizationally adaptable, innovative and thrive in high complexity environments to deliver high quality work product in the face of multiple demands
  • Broad experience working across multiple projects in the field of microbiology and the microbiome is preferred
  • Demonstrated ability to design and apply bioinformatics techniques to a complex biological question, leading to actionable hypothesis testing / validation is preferred
  • Demonstrated proficiency in programming languages (e.g. C++, Java, Python, Perl) is preferred
  • Demonstrated proficiency in analytical languages (e.g. R, Matlab) is preferred
  • Expertise in methods pertinent for functional interpretation of -omics data, e.g. pathway enrichment, functional module detection, causal reasoning is preferred
  • Experience with relational databases (e.g. SQL) is preferred
  • Experience with microbiome software (e.g. QIIME, Biobakery) is preferredClinical Research non-MD
57

Senior Scientist Resume Examples & Samples

  • Act quickly, lead and provide expertise and solutions for characterization of drug products and investigations on commercial products and R&D projects
  • Show ability to lead small scientific team
  • Apply state-of–the art analytical knowledge to ensure high quality of the delivered results
  • Work in a multidisciplinary team of researchers and show willingness to learn/explore new techniques
  • Develop test procedures and write scientific and investigations reports
  • Stay up to date with the scientific literature
  • Initiate and follow up collaboration with external partners and universities
  • Doctorate (Ph.D.) in Engineering; Chemistry (analytical/organic), Pharmaceutical Sciences or any related science/engineering field and minimum 6 years of experience in industry or equivalent
  • Prior experience in Pharmaceutical Industry is an asset
  • Show ability to lead scientific teams
  • Good knowledge and prior experience in one of the following scientific area is required: Rheology; Packaging and Devices testing, Extractable and Leachable; Polymer sciences; Foreign particle identification; Trace metals analysis
  • Ensure high scientific quality standards for experiments and take on responsibility for these experiments
  • Efficient, flexible and dynamic
  • Demonstrate capabilities in strategic thinking
  • Sense of Urgency
  • Good English scientific writing skills
58

Senior Scientist Resume Examples & Samples

  • Demonstrated skills in applications of mass spectrometry in a biopharma setting especially in regards to protein modification and chemical degradation and stability
  • Participating and heading up technology development initiatives and interacting with biophysical researchers to help extend and transform existing capabilities within the organization
  • Attention to detail and the overall quality of analytical results and the ability to work in a team-oriented environment are critical to this position
  • B.S./M.S. in chemistry, biophysics, biochemistry, engineering, or a relevant field with at least 6 years of experience OR a Ph.D. in chemistry, biophysics, biochemistry, engineering, or a relevant field with at least 3 years of experience is required
  • Postdoctoral experience is preferred
  • Experience in mass spectrometry including peptide mapping, proteomics as well as computational programming is required
  • Operating/programming automated liquid handling robotics systems to enhance high throughput sample preparation and analysis is preferred
  • Strong computational background and experience using informatics and computer programming to automate analyses is preferredR&D
59

Senior Scientist, Pharmacometrics Resume Examples & Samples

  • A minimum of a Master’s Degree with 8 years of experience OR a Doctorate degree (PhD or Pharm D) with a minimum of 3 years of experience in Pharmacokinetics, Pharmaceutical, Sciences or related field is required
  • A minimum of 3 years relevant industry experience, with focus on pharmacokinetics is also required
  • Knowledge of modeling and simulation components of reports and/or regulatory documentations for small molecules is also required
  • Hands on experience with a relevant Modeling and Simulation tool(s)/ software including WinNonLin, NONMEM, Berkley Madonna, R or SAS is required
  • Knowledge of other tools such as SimCyp and/or Gastroplus is preferred
  • Knowledge of PK/PD modeling for viral diseases is preferred
  • Ability to operate in a multicultural environment, participate in international teams and work independently is required
  • Strong technical, organizational, oral and written communication as well as teamwork skills is required
  • Ability to multi task and prioritize to delivery results within tight timelines is also required.R&D
60

Senior Scientist Resume Examples & Samples

  • A Bachelor’s Degree is required, preferably in Analytical, Polymer, or Organic Chemistry
  • A Master’s or PhD is preferred
  • 5 (five) years of relevant experience is required, 7 years’ preferred
  • Solid fundamental chemistry knowledge and the ability to identify the appropriate analytical methods and make relevant measurements to provide data and information that drive technical solutions is required
  • In-depth understanding as well as extensive hands-on experience in at least one common area of separation and quantitative analytical techniques are required
  • Familiarity with other characterization techniques such as spectroscopic techniques or polymer characterization is desirable
  • Technical writing, effective communication, and interpersonal/team work skills are required
  • Experience in Pharmaceutical or Medical Device industry is preferred.R&D
61

Senior Scientist, R&D Microbiology Resume Examples & Samples

  • A Bachelor’s Degree in a Microbiology or related biological science with a minimum of 4 years experience in medical device, pharmaceutical or consumer applied microbiology OR a Master’s with a minimum 2 years experience OR a PhD with 1 year experience is required
  • Training in environmental, clinical or industrial microbiology is also required
  • Excellent written and oral communication skills are required
  • Experience working in a GMP environment is strongly preferred
  • Knowledge in test method validation, industrial sterilization methods, controlled environments, or medical devices is strongly preferred
  • Willingness and ability to work in a project-driven, collaborative team setting in the medical device industry is required.R&D
62

Senior Scientist Resume Examples & Samples

  • Applies the understanding of (1) the impact of intra- and inter-subject variability in physiology and/or pathology, concomitant medication use, and biopharmaceutics, on pharmacokinetics (PK) and PK/pharmacodynamics (PD), and (2) requirements for the clinical pharmacology regulatory submission packages and submission processes
  • Carries out functional responsibilities in accordance to applicable SOPs, regulatory requirements and Johnson & Johnson Credo principles
  • Contribute to overall compound development via application of quantitative methods to integrate knowledge of PK, PD, patient characteristics, disease states, and drug-drug interactions to optimize dose selection, dosage regimens and study designs throughout drug development. With assistance from senior members, the TA Scientist CPPM will translate quantitative knowledge into strategic opportunities with key stake holders to drive development along the model-based drug development principles
  • Assist CPPM and PM Leaders with modeling and simulation activities in drug development programs. Perform and/or liaise for modeling and simulation analysis of preclinical-clinical data, translational PK/PD data, up to first-in-human (FIH) and if applicable beyond FIH (dose/exposure-response analyses to guide dose regimen from pre-proof of concept (POC) and POC studies)
  • Help design Phase I Clinical Pharmacology studies
  • Contribute to preparation of monographs, INDs and other documents as applicable to support clinical studies
  • Remain current with clinical and drug development information and methods in modeling and simulation by engaging with the scientific community (e.g., publishing, presenting at meetings, participating in special interest groups within professional societies, etc.) and internalize key learnings back to Janssen
  • Work effectively in matrix environment, managing CP deliverables in accordance with timelines and overall project goals
  • Apply relevant technical trainings/learnings to daily responsibilities, with focus of opportunistic deliver of value/impact
  • BS, MS, PharmD, PhD or equivalent degree in Pharmaceutical Sciences, Clinical Pharmacology, Biomedical Engineering, or relevant Biological Sciences. Ph.D. degree or equivalent, with 2+ years of relevant experience (including postdoctoral studies)or a MS or PharmD degree or equivalent, with 3+ years of relevant experience or a BS degree with 5+ years of experience performing progressively advanced duties
  • Understanding of overall process of drug development and the overall pharmaceutical R&D process
  • Has established a level of expertise and scientific reputation through publications and/or presentations
  • Drug development experience in one or multiple Therapeutic Areas and the ability to handle contributions to multiple clinical pharmacology programs, simultaneously
  • Demonstrated understanding of model based drug development (MBDD), biopharmaceutics classification system (BCS), and biostatistics principles and tools (e.g., Gastroplus, Simcyp, Winnonlin, NONMEM) and demonstrated ability to apply these tools to enable rational and efficient drug development
  • Understanding of PK, PD, PK/PD, and Translational Medicine
  • Working knowledge of US, European, and Asian (including BRIC countries) regulatory requirements and guidelines
  • Ability to interpret PK and PKPD results and prepare presentations to illustrate findings accurately
  • Working knowledge of clinical and regulatory landscape, disease processes and mechanisms, available treatment paradigms, and patient populations within assigned Therapeutic Area(s)
63

Senior Scientist, Discovery Preformulation Resume Examples & Samples

  • You will be expected to influence discovery project teams in finding NCEs with desirable pharmaceutical properties
  • You will need to define pharmaceutical developability assessment criteria, as they pertain to disease state, program biology and late-stage development needs, in collaboration with partners in discovery and development organizations
  • Perform analytical method development (HPLC/LC-MS) for small molecules and peptides in support of preclinical studies, including forced degradation analysis and elucidation of degradation mechanism
  • Conduct preformulation studies including but not limited to optimization and preparation of formulations for pre-clinical toxicological and PK/PD studies, solubility measurement, solid-state characterization using techniques such as, XRPD, DSC, TGA, and vapor-sorption analysis etc
  • Ph.D. with at least 3 years of industrial experience in Chemistry, Pharmaceutical Sciences, or related disciplines OR a MS with at least 6 years of industrial experience in Chemistry, Pharmaceutical Sciences, or related disciplines OR a BS with at least 10 years of industrial experience in Chemistry, Pharmaceutical Sciences, or related field is required
  • Analytical method development for small molecules with strong wet-lab experience is required
  • Experience in performing forced degradation studies is required
  • Experience in performing analytical method development for peptides is preferred
  • Experience in elucidation of degradation mechanisms of drug candidates is preferred
  • Experience in conducting preformulation studies is preferred
  • Experience in measuring solubility and performing solid-state characterization is preferred
  • Experience in applying novel formulation and drug delivery technologies to enable evaluation of drug candidates via oral and alternate routes in discovery and/or in development is preferredClinical Research non-MD
64

Senior Scientist, R&D Analytical Resume Examples & Samples

  • A minimum of a Bachelor’s degree in Chemistry, physical science or related discipline with a minimum of 5 years of professional experience OR a Master’s degree with a minimum of 3 years of professional experience OR a PhD is required
  • Experience with Analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, wet chemistry and compendia techniques in a cGMP environment is required
  • Strong technical written and verbal communication skills is also required
  • Ability to work in a team environment and to manage multiple deliverables with competing timelines is required
  • Experience with Empower, LIMS, developing Analytical test methods is strongly preferred
  • Experience with semisolids (emulsions, creams, lotions and/or gels) is also preferred
  • Experience working on cross-functional teams with Analytical, Microbiology, Procurement, R&D, Supply Chain, Operations, Manufacturing or other functions is preferred.R&D
65

Senior Scientist Solid Dosage Form Compaction Resume Examples & Samples

  • Execute formulation and process development activities in the area of solid dosage development with specific focus on the compaction process
  • Supporting scale up and tech transfer of the tablet compaction process in close collaboration with the Janssen Supply Chain
  • See opportunities for innovation, built further on the current compaction technology platforms and expand the most standard methodologies
  • Built up a strong relationship with collaborating departments and partners such as Pharmaceutical Sciences, Analytical Development, SM API development, Portfolio Management, Clinical Supply Chain etc.,
  • Use your global network for setting up collaborations with external partners and follow-up on Pharmaceutical Development activities
  • Follow-up literature (scientific and patent) in order to create new development opportunities for Pharmaceutical Development
  • Write and review of protocols and characterization reports
  • Build great relationships with Preclinical, Toxicology, Clinical Pharmacology, Therapeutic Area, Marketing, etc
66

Senior Scientist Resume Examples & Samples

  • Partner with scientists across the organization to apply antibody structural knowledge and statistics to analyze large number of antibody sequences for therapeutic antibody generation
  • PhD in computational biology or a related field with at least 2 years of Post-Doctoral experience is required
  • Demonstrated experience in quantitative analysis of high-volume biological datasets is required
  • Practical knowledge of statistical techniques is required
  • Proven critical thinking skills and the ability to consider outcomes when designing analyses
67

Senior Scientist, Data Sciences Resume Examples & Samples

  • Familiarity with many technologies and processes with a particular focus on their capabilities and limitations; in-depth knowledge of all areas of IT and the resources available to deliver projects or programs
  • Advanced knowledge of the business processes, data and strategic plans/initiatives of the Janssen Therapeutic Area functions (CVM, Immunology, Infectious Diseases, Neuroscience and Oncology)
  • Understanding of the business impact of different solutions, and the ability to assess and communicate the tradeoffs between business needs, technology requirements, costs, and risk
  • Understanding of departmental budgets and the ability to allocate resources accordingly
  • Strong expertise in health informatics, including familiarity with health outcomes databases, clinical trial registries; multi-lingual and cultural awareness
  • An advanced degree (Master’s, PhD or MD) with a minimum of 3 years of relevant experience OR a Bachelor’s degree with a minimum of 5 years of relevant experience in Computer Sciences, Statistics, Machine Learning & Artificial Intelligence, Molecular Biology, Bioinformatics, Computational Informatics, Medical Informatics, Computational Biology or a related discipline is required
  • Demonstrated knowledge of health informatics / health outcomes research and strong business analysis skills are required
  • Strong understanding of health care data standards such as OMOP, Snomed, ICD, LOINC, CDISC etc. is required
  • Strong understanding of and demonstrated expertise in health care data analytic methods / biostatistics is required
  • Experience with SQL or scripting is preferred
  • Knowledge of SDLC is preferred
  • Understanding of Health Outcomes research and trial design is preferred
68

Packaging Senior Scientist Resume Examples & Samples

  • BS in Packaging and/or Engineering/Science related degree
  • 4-6 years of work experience in leading & executing packaging projects. Food packaging experience is an advantage
  • Understanding of Customer and Consumer requirements, Supply, Marketing, Commercial, Sales
  • Ability to solve practical problems and deal with a variety of variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
  • Knowledge of packaging materials, packaging equipment, packaging systems, and distributions systems of truck, rail and warehousing
  • Ability to use Microsoft Excel, Word, PowerPoint, database management software, Lotus Notes and packaging design software such as TOPS and/or CAPE and AutoCAD design software
  • Understanding of ASTM and TAPPI test procedures that apply to food packaging
  • Project planning and management skills
  • Creative, value-added thinking, scenario thinking
69

Process Development Senior Scientist Resume Examples & Samples

  • Develop key new technologies and processes to enable the global rice and grains battlefield with a focus on the Blending technology platform and concentration on dry
  • Drive development of process specifications, integration and training for PPPI teams
  • Partner with Flavour New Product Development and Format Teams to ensure a seamless implementation transition from new product concept to production
  • Develop and execute the supporting trial plan and risk management process for new product and process implementation
  • Directly and indirectly develop new processes and improve existing to provide new product capability, deliver higher product quality, or improve manufacturing efficiency
  • Lead multi-disciplinary teams responsible for innovation projects from concept to execution
  • Represent Blending/Process Development in various multi-disciplinary teams/projects to ensure all process considerations are met
  • Manage projects conducted by external research providers and where applicable the related Food Technology Platform budget allocation
  • Successfully implement major process upgrades by working closely with the Engineering team to design and commission new process equipment and modifications to existing
  • Provide process and product support to the Manufacturing department through an intimate technical knowledge of process and product design
  • Ensure all new processes and process modifications meet global standards by leading and participating in HACCP studies and executing any actions relating to process design, commissioning or training
  • Recipe Implementation – Setup and commercialization, lead pilot scale trials through factory scale-up (including new process validation), recipe review and optimization based on Quality results & other inputs
  • Process Development – Design, HACCP, commissioning and hand-over of new process equipment
  • Contributor and decision maker in FMOS forums
  • Provide qualification of new rice and grain varieties and adaptation to current and future portfolio needs
  • Manage intellectual property, invention, patents and portfolio compliance
  • Identify efficiency opportunities and bring them to life through globally applicable standardized process technologies
  • Provide leadership to design for quality and efficiency apply Lean and Value Added Engineering principles
  • Use scientific practices and fact based validation techniques to scale-up and deploy
  • Deliver new product and process innovation areas and concepts through rapid prototyping
  • Use experimental design discipline to execute solutions, improve manufacturability of current products, and reduce overall cost
  • Chemical and Process Engineering Aptitude
  • Mechanical Aptitude
  • Numerical Analysis
  • Process Control Understanding
  • Engineering - See R&D capability framework; anchor role: Individual contributor knowledge generation & translation
  • Knowledge of Mars quality systems and lean manufacturing principles preferred
70

Maltesers Innovation Senior Scientist Resume Examples & Samples

  • Lead global product harmonization programme enabling cross sourcing and understanding the interaction between product & consumer
  • Support product and recipe validation with new technology development from project initiation through to full scale execution
  • Perform and manage trials at pilot plant and full factory scale
  • Actively support global CI and capacity expansion work working with the regional teams
  • Manage consumer investigations to develop greater understanding
  • To identify, develop and improve the Maltesers® recipe, process and production methods across all current and future sites to recommend a standard approach for the efficient production of Maltesers®
  • To influence the global supply network whilst delivering a harmonized product, support setting regional strategies to deliver step improvements to the line/brand performance
  • To identify future opportunities for efficiency, quality and or growth through recipe & product innovation
  • To lead global consumer testing to validate a global single product specification
  • To consult as Maltesers expert on complex growth projects at production sites
  • A strong drive for results
  • Great problem-solving capabilities
71

R&D Senior Scientist Resume Examples & Samples

  • University degree in Food Science, Food Technology or Food Engineering
  • Demonstrable experience of practical application of practical application in Product/Process
  • Development within Chocolate and commercialization of one or more product/process(es)
  • Good knowledge on chocolate manufacturing technology and ability to operate the equipment
  • Excellent project management and organizational skills, with a focus on delivering results
  • Previous experience of running trials
  • Demonstrable ability to engage stakeholders and work cross-functionally
  • Flexibility and stress resistance whilst managing work load within a tight time frame
  • Fluency in English required, other language skills (French, German) are beneficial
  • Flexibility to travel
72

Rd&q-senior Scientist Resume Examples & Samples

  • Independently design and develop products & processes for large to major sized projects, including those with multiple business partners, in order to deliver against the project objectives either in relation with
  • University Degree in the area of food science, engineering, food technology or other relevant subject
  • 7+ years of R&D and/or Quality experience (ideally in Savory snacks / Biscuit Industry)
  • Thorough understanding of food products science/processing/quality (Savory snacks / Biscuit raw materials and processes knowledge a plus)
  • Strong creative mindset and passion for Savory snacks in order to drive creative products and process solutions
  • Demonstrate high Project Management & Leadership skills
  • Ability to communicate and collaborate in international environment efficiently and to build strong crossfunctional relationships
  • Capability and willingness to work independently and to solve problems on your own
  • Willingness to travel (around 25% of time)
73

Rd&q-senior Scientist Resume Examples & Samples

  • 5 years of experience in FMCG industry, including min. 2 years of experience in a plant (in Quality, Production or Continuous Improvement). Continous Improvement experience will be a plus
  • Thorough understanding of food products science/processing/quality
  • Experience of SPC tools (Statistical Process Control) as a plus
  • Experience of SAP in Quality Management (SAP QM “Quality Management” & SAP QN “Quality Notification”) as a plus
  • Willingness to travel across Europe (for around 25% of time)
74

Senior Scientist Resume Examples & Samples

  • Provide high quality customer service at all times by ensuring effective organisation of assigned workload, integrity of analytical data and timely/accurate provision of results
  • Work to the highest standards of safety and quality by ensuring that appropriate COSHHs, risk assessments and SOPs are understood and followed
  • Provide technical direction within own area of expertise within the team whilst independently performing a range of GMP analyses using wet chemistry techniques
  • Perform data checking and provide interpretation of results for routine and verification testing
  • Generate certificates of analysis or external interpretive reports
  • Provide effective line management of a small team of junior staff
  • Provide training and supervise junior staff in routine activities following pharmacopoeia and client methods
  • Take responsibility for specific project management and specific areas of general laboratory/sample administration and assignment of housekeeping tasks as required
  • Liaise with clients, business development and line management to ensure effective communication of project proposals and results
  • Write and approve SOPs and test methods
  • Educated to Degree or PhD level in Chemistry or alternative relevant scientific discipline or have equivalent relevant experience in a laboratory
  • Excellent understanding of basic laboratory equipment
  • Scientific understanding and ability through extended experience to independently conduct chemical analysis using wet chemistry techniques
  • Thorough understanding of pharmacopoeia and pharmaceutical testing requirements
  • Previous experience working within a GMP contract laboratory
  • Line Management experience, with strong examples of people development
  • Strong verbal and written communication skills in English, with the ability to effectively network with external clients and internal teams
  • Excellent organisational skills including time management and priority setting
  • Meticulous attention to detail, well organized with a strong team working ethos
75

Senior Scientist Resume Examples & Samples

  • Degree in Food Science and Technology (or similar) - such as degrees in the area of Science, Nutrition, Health and Technology
  • Experience including representation and negotiation capability in associations
  • Good knowledge of the local Regulations in both Philippines and Indonesia including interpretation and its implementation
  • Good knowledge of Mondelez business, i.e. market environment and Mondelez trade position as well as Mondelez manufacturing processes and portfolio
  • Knowledge in the areas such as Product Development, Quality, and Nutrition
  • In depth understanding of BPOM registration requirements and Halal registration requirements and procedures
  • Working knowledge in international Food Regulations / Law
  • Minimum 4 years of working experience in SARA and / or related RD&Q areas
  • At least 4 years of experience in representing the company in industrial associations driving aligned positions following code of conduct
76

RDQ Senior Scientist Resume Examples & Samples

  • Provide scientific and technical food safety and microbiological support to the BU/Region to ensure product safety and quality by conducting assessment of existing suppliers/co-manufacturers. Identify and communicate micro food safety risks to BU/Region, giving actionable advice on Food Safety and Microbiological programs
  • Conduct validation review of Critical Control Points related to heat kill steps (cocoa, nut processes etc) and assess validity of data obtained by others
  • Review process validation – involves review of the technical validity of data generated to validate kill steps, and review other food safety programs: HACCP, zoning, PEM, allergen and physical hazard controls
  • Perform Supplier Food Safety assessments for suppliers, co-manufacturers and Mondelēz facilities (laboratories are not included, unless located at the suppliers’ site) and provide them with recommendations on methods/techniques
  • Work closely with the auditing group to validate/verify Food Safety and Microbiological programs at supplier, co-manufacturers and Mondelēz facilities and recommend approval or disapproval to ensure brand protection & contribute to business growth
  • Partner with business partners (e.g. Supplier Quality and Procurement) where improvements and execution of relevant HACCP models, PEM and other food safety programs are required at external facilities
  • Continuously improve micro & food safety related knowledge, skills and understanding of food microbiology, epidemiology and food hygiene matters
  • Continuously improve performance by upgrading skills and identifying/using skill-enhancing assignments, courses and training opportunities, as well as networking opportunities to ensure up-to-date knowledge
  • Co-manage the selection process for Supplier Food Safety Assessments (SFSA) in the Mondelez regions by analysis of Supplier self-assessments and prioritizing visits, based on food safety risk profiling
  • Responsible with other team member for scheduling and performing SFSA visits
  • Provide input into review and up-dates of global documents e.g. Dairy processing expectations, -Egg processing Expectations, Fruit and Vegetables processing review, and the Supplier HACCP manual review
  • Training/educating suppliers in identifying critical parameters of processes used, the mechanisms underlying control steps and the measurements needed to validate these processes when requested by other functions (Supplier Quality)
  • Provide technical support and training to the food safety and audit teams in other regions
  • Involvement in Global Food Safety calls and active input on food safety topics in order to align internally between different regions
  • Knowledge of HACCP and awareness of ISO 22000
  • Knowledge of Microbiology Laboratory Techniques with awareness of rapid test methods
  • Experience with validation of Critical Control Point (Lethality steps such as roasters, cookers)
  • Demonstrated ability to work with computer systems to enter, analyze and report information
  • Ability to apply technical know-how to understand and develop products/processes
  • Good command of English- both written and spoken
77

Senior Scientist, Nutrition Resume Examples & Samples

  • You will have to build research programs (including in vitro, and/or animal and/or human trials) to promote specific dietary lipids for specific interest in Mondelez. It will require to identify and lead collaborations with external laboratories (academic or private) to manage the trials to participate to the nutrition strategy of Mondelez and build future innovations
  • You will have to identify health implications in dietary lipids to provide recommendations in food product formulations, to participate to the improvement of nutritional profiles of Mondelez portfolio
  • You will have to collaborate closely with Ingredient Research team to build shared programs on novel lipids to evaluate their nutrition interest and safety issues for innovations
  • You will have to collaborate closely with the other nutrition researchers who work on carbohydrate metabolism to provide new insights related to lipid interferences
  • You will have to participate to external meetings and congresses in the area of dietary lipids to show Mondelez research work externally and to collect opinions, interest from academics
  • You will have to communicate internally your results in team meetings and in larger transversal meetings to promote nutrition research work and to collect feedbacks from others
  • Doctorate is a plus
  • General Work Experience : Nutrition Research area (physiology, cell biology) min 2 years
  • Functional Work Experience: Dietary Lipid research min 2 years
  • Statistical skills
  • Proactive
  • Good business understanding,
  • Communication and negotiation skills
  • Strong ability to work in transversal teams
  • Fluent in English and have a good command of French language
78

Senior Scientist, Nutrition Resume Examples & Samples

  • You will participate to research programs (including in vitro, and/or animal and/or human trials) to promote specific dietary sugars for specific interest in Mondelez. You will participate in the identification of new collaborations with external laboratories (academic or private) to manage the trials which participate to the nutrition strategy of Mondelez
  • You will have to identify health implications in dietary sugars to provide recommendations in food product formulations, to participate to the improvement of nutritional profiles of Mondelez portfolio
  • You will have to collaborate closely with Ingredient Research team to build shared programs on novel sugars to evaluate their nutrition interest and safety issues for innovations
  • You will have to collaborate closely with the other nutrition researchers who work on carbohydrate and lipid metabolism
  • Functional Work Experience: Dietary Carbohydrate research with a specific interest in sugars, sugar alcohol, min 1 year
79

Senior Scientist Resume Examples & Samples

  • Stay at the forefront of the rapidly evolving microbiota research field, and identify microbiota questions embedding an integrative view of the gut ecosystem
  • Develop a mid-long term strategy for projects within the gut ecosystem research unit, and propose nutritional concepts able to promote health via the human-associated microbiota
  • Provide scientific support to business-related activities, engage and collaborate with stakeholders internally and externally
  • Develop and lead projects and deliver results in research activities in a timely and reliable fashion
  • Coach younger scientists and technicians
  • PhD with proven scientific expertise in the microbiota field, including knowledge in human microbial ecology
  • At least 3 year experience in Research and Development in a related field
  • Experience in microbiota analysis, biological interpretation and data integration
  • Bioinformatics scripting skills will be considered a strong advantage
  • Ability to steer and manage research projects and to lead teams on a project basis
  • Fluent in English, French would be an asset
80

Senior Scientist Resume Examples & Samples

  • Ensure that the statistical procedures are in accordance with Good Clinical, Epidemiological, and Pharmacovigilance Practices (GCP, GEP, GVP), other guidances and regulatory requirements for safety reporting. Ensure the quality and integrity of the reporting, for the pre/postmarket products
  • Be accountable for the data processing, biostatistical aspects of the safety analysis and reporting/signal detection related to the product
  • Develop project plans and implement timelines so that the reporting/activities related to safety analysis have been performed and delivered on time
  • Apply appropriate biostatistical principles, data structures, techniques and practices to assess safety/signal detection
  • Generate, review, and support safety documents and reports required for regulatory submissions/safety investigations
81

R&d-professional & Technical Affairs Senior Scientist Resume Examples & Samples

  • Scientific education with advanced degree preferred in life sciences (e.g., MD, PharmD, PhD)
  • Experience in the healthcare industry preferred – at minimum, experience in a regulated category
  • Ability to: Rapidly acquire knowledge & understanding of therapeutic category including physiology & pathophysiology; Analyse scientific & clinical data/information; Translate data/information into business relevant language & messaging
  • Pragmatic, open-minded, and creative approach to managing issues and problems
  • Excellent written & oral communication skills. Must have experience giving oral presentations
  • Strong and effective working relationships with external medical experts, thought leaders, and scientific organisations preferred
  • Ability to travel in support of market research and scientific events
  • Just apply via clicking the button below
  • Have your CV in English ready to attach (include examples of the challenging experiences you have had both within and outside academia)
  • Attach a summary of your latest grades
  • Please note individual attachments cannot be larger than 500 KB
82

Btec Senior Scientist Resume Examples & Samples

  • Deliver courses to North Carolina State University undergraduate and graduate students in subject matter related to gene expression systems and cell line development related to biomanufacturing. Specific topics include but are not limited to expression systems (e.g., bacterial, yeast, mammalian), DNA cloning, cell transformation and optimization of protein expression
  • Deliver short courses to industry professionals. Specific subject matter topics include but are not limited to expression systems (e.g., bacterial, yeast, mammalian), DNA cloning, cell transformation and optimization of protein expression
  • Develop cell lines for expression of proteins for use in courses and bioprocess/analytical services projects
  • Advise/mentor undergraduate and graduate students in bioprocessing projects
  • Conduct and/or provide planning support to projects under BTEC’s bioprocess or analytical services program or projects that are internal to BTEC
  • Communicate as needed to service providers, clients, and collaborators within and outside the University
  • Write grant proposals that provide funding for technology development, educational initiatives, etc
  • Publish and/or present
  • Gain local (within the state) recognition
  • Provide leadership to BTEC, particularly in the areas of molecular biology and cell line development
  • Actively promote BTEC locally (within NC)
  • Perform any other tasks/responsibilities assigned by supervisor
  • Proficiency with MS Office suite, specifically MS Word, MS Excel, and PowerPoint (or similar)
  • Good written and verbal communication skills, and particularly the ability to present information clearly and concisely in oral and written form
  • Good interpersonal skills and the ability to work with students from the university and from industry
  • Knowledge of laboratory safety and biosafety practices
  • Ph.D. in a life science (biochemistry, chemistry, microbiology, cell biology, genetics or related discipline)
  • Prior experience in teaching at the college level
  • Experience that led to successful completion of a cell line development project
  • Cell line development experience in a biopharmaceutical environment
83

Senior Scientist Resume Examples & Samples

  • Excellent professional and technical skills; ability to work with other employees and clients. Viewed as a knowledgeable resource in your field of expertise
  • Good understanding of project and professional services procedures. Ability to think creatively and be innovative in your area of expertise
  • Strong written and verbal communication skills required. Strong business development and selling skills
  • Provide technical services to Task Managers, Project Managers, Business Practice Managers and his or her Area Manager. Possess strong negotiating skills and a demonstrated ability to develop new clients, markets and services
  • Solicit the help and personal involvement of the Project Manager, Business Practice or Area Manager, as appropriate, to solve scheduling or technical problems within his or her area of expertise that are encountered in the progress of the work
  • Assisting with construction cost estimation, and field work consisting of construction oversight/management and field sampling activities
  • Working with subcontractors, setting up contracts, and managing day-today activities on large construction/remediation projects
  • Traveling to various sites to direct field activities and evaluate project progress, schedule, and budget
  • Conduct project research, technical editing, document development and production activities as assigned by the Project Managers
  • Assists in the preparation of proposals and cost estimates and becomes involved with client communication and development activity with direction and assistance from Project Managers
  • Inform Task Managers, Project Managers or Business Practice or Area Manager about the capability and performance of the employees assigned by them to his or her area of expertise on the projects
  • Remediation work for oil and gas companies considered a plus
  • Oil and Gas Field Equipment inventories and inspections
  • Oil and Gas Permitting and Compliance, RCRA/NPDES Permitting and Compliance
  • Minimum years of experience: 10
  • Bachelor’s Degree in engineering, science or related profession
  • 40 hour OSHA HAZWOPER
  • 8 hour OSHA Supervisor training
  • Registrations/Certifications Preferred: 10 hour OSHA construction
  • Training Behavioral based safety experience (Loss Prevention Systems (LPS) a plus), CPR and First Aid certification desired
84

Senior Scientist Resume Examples & Samples

  • Coordinate logistic activities for Hit Identification
  • Develop tracking and visualization tools for the hit identification portfolio for the purposes of portfolio reporting and transparency for Lead Discovery scientists and our partners
  • Provide metrics to the Lead Discovery leadership team for performance tracking and process optimization
  • Manage automation scheduling and apply automation expertise to meet scientific deliverables
  • Act as Janssen point-of-contact for in-sourced research performed by third-party providers
  • Manage external collaborations, including work conducted at contract research organizations
  • B.S. in biochemistry, biology or related areas with at least 12 years pharmaceutical research experience OR a M.S. in biochemistry, biology or related areas with at least 8 years pharmaceutical research experience OR a Ph.D. in biochemistry, biology or related areas with at least 5 years pharmaceutical research experience is required
  • Proven ability to coordinate and prioritize experimental laboratory activities is required
  • Proven ability to organize and present information using tools such as SharePoint, Tableau or Project is required
  • Proven ability to manage research activities of external research providers, either outsourced or insourced, is required
  • Familiarity with HTS or protein science workflows is required
  • Experience with automation platforms is required
85

Senior Scientist Resume Examples & Samples

  • Bachelor’s degree with 10 years of relevant programming experience
  • In-depth understanding of EO/IR sensor systems (tracking and discrimination) and seeker performance
  • Knowledge of FORTRAN Strong math skills necessary to develop and understand complex, state-of-the art algorithms
  • Strong programming skills, generation/modification, for new and existing codes
  • Ability to work cooperatively on a team and build effective relationships
  • Candidate must be able to obtain a Secret security clearance
  • Master’s degree with 10 years specific experience in IR Discrimination and seeker performance 10 years of relevant programming experience
  • Experience with elements of Missile Defense capabilities in the following areas; Weapons IR seeker systems; EO/IR sensor systems
  • Knowledge of C/C++/Matlab/Mathematica/Scripting languages is desired
  • Experience in Laser directed energy weapons
  • Knowledge of Linux/Unix commands
86

Senior Scientist Resume Examples & Samples

  • Provide subject matter expertise to a China-based team focusing on water monitoring market by leveraging his extensive knowledge and experiences in the area of water analysis including waste water, surface water and process water
  • Orchestrate and lead scientific feasibility investigation in ideation and definition phases of new projects by leveraging in-depth understanding of customer use cases and providing scientific evaluations to help make go/no go decisions about design choices for product under development
  • Provide development directions to guide R&D engineering activities throughout NPD to ensure successful delivery of products that thoroughly meet customer needs
  • Build and operate a professional network of key opinion leaders to provide insights and directions for water analytical instrument development at CIC
  • Work with product marketing function to define the new product development roadmap of water instruments for CIC with a forward looking view of future market opportunities
  • Represent Thermo Fisher Scientific as we interact with key opinion leaders in the forefront of developing national or industrial water monitoring standards, policies and regulations
  • Master/Ph.D. degree in analytical chemistry, environmental sciences (could include biologist with strong chemistry background), or possibly chemical engineering
  • >5 years of experience in water analysis
  • In-depth domain knowledge in water instrument development with established professional standing in water analysis or environmental analysis. A strong record of peer review publications is a strong positive
  • Excellent analytical, problem solving/decision making skills with the ability to make timely, effective and fact-based decisions
  • Adequate knowledge and resources to establish & operate an opinion leader group
  • Excellent communication skills both in oral and in written Chinese with the capability to effectively communicate key points and articulate proposals to the senior management
  • Strong self-motivation with the willingness to take challenges
  • Experiences in cross countries and cross cultures projects
  • Good communication skills both in oral and in written English
  • Experiences in technical innovation leadership position
87

Senior Scientist Resume Examples & Samples

  • Take charge in originating, applying, and documenting new analytical methods and techniques to solve problems in research and development and to support existing chemical manufacturing processes and products
  • Review existing documentation (test methods, instruction manuals, application notes, web content) in order to issue product updates
  • Update specifications and test methods to ensure chemical products are compliant with ongoing change criteria from pharmacopeia (USP, EP, BP, JP, NF)
  • Design, implement, and execute critical experiments associated with a research plan to develop new products
  • Deliver technical presentations and written reports/publications (in-house and peer-reviewed) of new products/applications
  • Manage multiple projects involving cross functional teams (operations, marketing, and sales) within a stage-gated process
  • Monitor research trends to ensure leading edge development of relevant reagent chemicals
  • Achieve a leadership role in the field of separation science both within Thermo Fisher Scientific and with the external scientific community
  • Doctoral degree (PhD) in Analytical/Bioanalytical/Organic Chemistry or BS/MS with equivalent related experience
  • 4 to 8 years of relevant work experience (industry experience preferred)
  • At least two publications (first author) in peer-reviewed scientific journals or patents (inventor or co-inventor)
  • Broad-based knowledge and experience in chemical analysis, experimental design (DOE), and statistical quality control
  • Excellent problem solving capabilities, strong interpretative data analysis, and high degree of computer literacy
  • Demonstrated interpersonal and networking skills by mentoring individuals, team participation, group teaching, seminar/poster presentations, and customer communication
  • Project management skills preferred
  • Significant experience in the field of separation science with emphasis on advanced chromatography and mass spectrometry systems (HPLC, LC-MS, GC, and IC). Specific experience using Thermo Scientific, Agilent, or Waters chromatography and mass spectrometry instrument systems
  • Significant experience with spectroscopy instrumentation such as UV-VIS-NIR and fluorescence spectrophotometers, NMR, Raman spectrometer, FTIR, and ICP-OES/MS
  • Ability to handle timelines and multi-task
  • Demonstrated dependability, team player, and positive attitude
88

Senior Scientist Resume Examples & Samples

  • Interact with formulators and Product Performance Managers (PPMs) to determine the consumer testing and consumer knowledge needs of the skincare lab
  • Design and execute consumer studies, specifically qualitative and quantitative consumer tests from inception to completion with quality, timeliness and professionalism
  • Test the relationship among consumer sensory perception, expert panel results and instrumental readings
  • Draft screeners for recruitment and work closely with Logistics team to ensure proper recruitment is completed
  • Design and execute lab and field observational studies on how consumers apply/use skincare products and evaluate product satisfaction
  • Conduct one-on-one interviews concerning the sensory attributes of products and consumer attitudes, beliefs and behaviors
  • Prioritize project workload with R&I team
89

Analytic Science Senior Scientist Resume Examples & Samples

  • Lead technical architecture and design process
  • Keep a critical eye on new design specifications and raise quality standards, address architectural concerns
  • Provide technical leadership and mentoring to product development team
90

Senior Scientist Pharmacokinetics Resume Examples & Samples

  • PhD in a relevant life science discipline
  • A fundamental understanding of drug discovery and development and the role of pharmacokinetics
  • In-depth training and hands-on experience in pharmacokinetics and basic knowledge in mechanistic PK-PD (TK-TD) modeling
  • Additional experience in absorption, distribution, drug metabolism, enzyme kinetics and transporter research is highly desirable
  • Ability to design, supervise and interpret various types of mechanistic ADME/PK and TK studies
  • Proficiency in the development/optimization of new/existing experimental models to support hypothesis driven pharmacokinetic research
  • Prior experience with PK analysis (non-compartment & multi-compartment modeling) and a demonstrated ability to work with modeling tools (e.g. NONMEM, Phoenix, GastroPlus, SimCYP)
  • Active scientific participation and collaboration with colleagues in industry, academia and regulatory agencies
  • Strong analytical thinking, excellent communication skills and the proven ability to work independently as well as effectively within a team environment
91

Senior Scientist Resume Examples & Samples

  • Conducting literature and patent searches
  • Organizing and assimilating results of literature searches
  • Design of experiments; data acquisition, analysis, and interpretation
  • Chemical and material characterization
  • Development of measurement techniques and models
  • Prototype formulation development for proof-of-concept studies
  • The selected candidate must be able to work in and leverage resources in a global, highly networked environment
  • The Sr. Scientist will work closely with internal R&D partners and external collaborators to define project objectives and timelines and execute projects
  • A minimum of a Bachelor degree is required
  • A minimum of 4 years professional experience is required
  • A degree in Chemistry, Biochemistry, Chemical Engineering, Materials Science, Biomedical Engineering, Pharmaceutical Sciences or a related major is required
  • Experience with measurement science techniques (e.g. Confocal Microscopy, QPCR, Raman, FTIR, AFM, Zeta Potential, Chromatography, Surface Analytical Techniques) is required
  • Formulation or bacterial biofilm model development is preferred
  • Previous product development experience in the consumer products or healthcare products industry is preferred
  • Technical experience in the fields of surface chemistry, bio physical chemistry, bio analytical chemistry or material chemistry are preferred
  • Candidates with previous experience working with external material or technology providers (e.g., suppliers, external manufacturers, incubators, inventors) are highly preferred
  • Previous experience coordinating the work of contractors or laboratory technicians is also preferred
  • Experience in physical, chemical, in-vitro or clinical studies is preferred
  • Excellent oral and written communication skills and solid presentation skills are required
  • The candidate must be able to work independently on multiple projects AND able to successfully partner and influence cross-functional team members
  • Technical writing and publication is required
  • This position may require up to 10% overall travelR&D
92

Senior Scientist, Oils Resume Examples & Samples

  • Drives Creativity and Innovation: Formulate and develop products intended for consumer use
  • Builds Collaborative Relationships: Will need to work closely with Market Research, Product Development, and other product formulators; work closely with suppliers to source new fats and oils with appropriate characteristics/qualities and lipid profiles
  • Strives for Excellence in Execution
93

Senior Scientist Resume Examples & Samples

  • Collaborate with Therapeutic Area Safety Head (TASH)/MSO/Safety Surveillance Physician (SSP) and other stakeholders on strategy development
  • Initiate/Conduct/Oversee searches of internal and external databases
  • Perform and/or lead aggregate safety analysis and case level review
  • Author, contribute, and coordinate the preparation of core safety deliverables
  • Ensure commitments (e.g., Pharmacovigilance Agreements (PVAs), assessment reports) are met
  • Partner with vendor to develop reports/deliverables
  • Provide SMT support as needed
  • Act as ad hoc member for assigned products as appropriate
  • Participate in cross-functional training of relevant stakeholders
  • Act as product or process Subject Matter Expert (SME) during audits/inspections
  • Participate or lead department and/or cross-functional initiatives
  • Recognize potential issues and or safety issues and escalate to the attention of the report owner, line manager, or MSO
  • Ability to understand nature of adverse drug reactions and complex associations
  • High level of flexibility and ability to (re)prioritize work of oneself and others
  • Attention to detail and ability to analyze data in broader context
  • Ability to work across multiple functions and therapeutic areas
  • Review regulatory assessor comments/requests and accommodate/address as appropriate with guidance
  • Bachelor’s Degree in Health or Biomedical Science and a minimum of 6 years pharma industry experience is required
  • Advanced Degree Preferred in Health or Biomedical Science and a minimum of 4 years pharma industry experience is preferred
  • A minimum of 1 year Clinical/Medical writing or PV experience is required
  • Strong English verbal and written communication skillsDrug & Product Safety Science
94

Senior Scientist Resume Examples & Samples

  • A Bachelor’s degree in Chemistry, Pharmaceutics, Engineering, or related area is required
  • A minimum of 8 years of experience in business is required, including a minimum of 5 years of pharmaceutical development or pharmaceutical manufacturing experience
  • Knowledge of both pharmaceutical product R&D and/or Technical/Site Operations functions and experience, including large molecule drug product processes and manufacturing, is preferred
  • Experience with introduction of pharmaceutical products to manufacturing sites and late state development with working technical knowledge of manufacturing site unit operations is required
  • Demonstrated leadership in providing integration of activities and information across multifunctional groups and matrix teams is required
  • Ability to foster team productivity and cohesiveness and to work collaboratively to execute, deliver and get results through the various matrix teams is required
  • Planning and logistics skills capable of effective integration of drug substance deliverables and support of detailed execution at the manufacturing site level are preferred
  • Knowledge of manufacturing site systems and procedures (SAP, electronic batch records, cleaning, material handling, etc…)
  • Statistical SME and/or Six Sigma experience and certification preferred
  • Excellent written and oral communication skills and ability to influence peers, superiors, and partners in a global environment
  • Motivated, self-starter able to work independently with demonstrated problem solving skills
  • Be able to sit in Malvern, PA, Horsham, PA, Raritan, NJ, or Spring House, PA and be open to 25% domestic and international travel.Process Engineering
95

Senior Scientist Resume Examples & Samples

  • Accountabilities
  • Develop innovative biscuit product formulations
  • Work closely with regional counterparts, build relationships and network across regions and represent global R&D function in team meetings
  • Understanding of ingredients’ functionality and testing of new ingredient technology from key suppliers for next generation of product improvements
  • Coordinate sensory and analytical testing of prototype formulas
  • Ability to synthesize data from a wide variety of sources and apply training to draw logical conclusions
  • Design and conduct stability studies to ensure adequate shelf life for new formulations
  • Transfer new formulations to the pilot plant for manufacturing scale-up (commercialization) together with process development lead
  • Assessment of competitive products and technologies
  • Maintain a detailed laboratory notebook and record all laboratory experiments
  • Assist in maintaining all laboratory equipment and ensure compliance with established safety standards / practices for laboratory, pilot plant and the STC facility
  • Create and manage specifications
  • Ability to work collaboratively with cross-functional teams and comfortable in a multi-cultural and complex global environment
  • Pre-requisites
  • Ability to work collaboratively with cross-functional teams and internal RD&Q clients and colleagues while providing technical input on all projects
  • Build and establish business partnering skills with RD&Q, Supply Chain and Marketing group
  • Excellent oral and written skills and have the ability to present technical findings to team
  • Learning agility and ability to deal with high levels of ambiguity
  • Proficient use of Microsoft office and Outlook email system
  • B.S in Food Science/Food Engineering/Chemistry/Chemical Engineering with six or more years of RD& Q/Manufacturing experience (food industry preferred). Master’s degree with 4 or more years of experience
96

Global Chocolate Q&FS Senior Scientist Resume Examples & Samples

  • Knowledge/Experience
  • Strong working knowledge of Quality Management Systems, including the Mars Quality Management Process (QMP), ideally gathered through implementation of QMP at BU or site level
  • Strong working knowledge of Food Safety Management Systems, including HACCP, ideally with experience of implementing HACCP programme on a site
  • Preferred: Formal training as an internal auditor
  • Understanding of Inbound (Supplier) and Outbound (Distribution) Supply Chain processes
  • Knowledge of food safety, food processing, raw material supply chains, risk assessment and food safety regulation/legislative requirements
  • Strong organizational skills and demonstrated ability to successfully handle multiple projects
97

Senior Scientist Resume Examples & Samples

  • Prepares cost and schedule estimates and technical documents on proposed projects in assigned area
  • Demonstrates creative ability through patent disclosures; problem solving; scientific reports or technical papers and articles
  • Participates in special projects as required
98

Senior Scientist Resume Examples & Samples

  • Ph.D. in a biomedical science (preference molecular and cellular immunology) from an accredited college/university according to the Council for Higher Education Accreditation (CHEA)
  • Minimum of five (5) years post-graduate experience
  • Project management experience in a research setting
  • Experience with biochemical/immunological assays including: ELISA, Western Blot and immunoprecipitation, over expression or knockdown of gene of interest
  • Expertise in cellular and molecular biology
  • Experience with evaluation of anti-viral or cytotoxic effect, gene silencing, and fluorescence activated cell sorting (FACS)
  • Expertise in viral pathogenesis
  • Attendance and presentations at national meetings
  • Multiple first/senior authorships on peer-reviewed publications in immunology, virology or biology field
99

Senior Scientist Resume Examples & Samples

  • Be a recognized leader with a national or international reputation for battery research and development
  • Be tasked with leading battery research, developing partnerships with other national labs, industry and academia in an effort to advance and enable energy storage technologies
  • The scientist will join a team of over 40 world-class scientists and engineers with a diverse portfolio
  • Work closely with DOE sponsors and industry to accelerate the development and deployment of new technologies for transportation and electrical grid-scale energy storage and enable continuous power from renewable energy sources
  • Develop and execute technical strategies to strengthen PNNL's technical capabilities in batteries & energy storage
  • Provide leadership to the Laboratory in executing internal initiative investments in energy storage, along with technical leadership in the conception and execution of innovative research programs
  • Lead and support efforts to grow externally funded research programs in batteries and energy storage. This includes the ability to establish and grow relationships with key clients and collaborators in industry, academia and other national laboratories, as well as leading the development of research proposals
  • Build strong multidisciplinary R&D teams to meet project deliverables and impact the key scientific and technological challenges in energy storage
  • Work closely with DOE program offices and industry
  • Mentor junior scientists and attract new talent to PNNL
  • Contribute to organizational goals, including contributing to PNNL strategic planning and prioritizing research objectives
  • PhD in Chemistry, Electrochemistry, Chemical Engineering, Material Science or related and 5+ years of experience
  • Industry experience is desirable
  • The Senior Scientist position must have an extensive publication record, including authoring seminal reports and publications, and delivering keynote addresses at relevant national and international forums
  • A demonstrated track record of initiating new research directions, directing innovative research and development programs, establishing strong client relationships, leading interdisciplinary teams, and attracting R&D funding
  • A strong orientation toward advancing the state of the science, demonstrated ability to work across multiple organizations to achieve scientific advances, and a strong publication record in relevant technical areas
  • Strong leadership skills to develop vision and strategy, effectively execute program development, and attract, mentor and develop talented staff
  • Strong oral and written communications are required to convey a vision and strategy to research teams, peers, and others who influence initiative and program decision-making
  • Widely recognized authority in energy storage and or batteries related research whose technical contributions are recognized as having a substantial impact on advancing the current state of knowledge and understanding of electrochemical energy storage systems
  • Demonstrated excellent track record in scientific publications or intellectual property development
  • Must have demonstrated experience developing and leading innovative R&D programs of significant size and impact across multiple institutions from industry, academia and national laboratories
  • Demonstrated leadership of multidisciplinary efforts to provide solutions to complex problems where the problems are characterized by lack of precedents, source material, or lack of prior success
100

Senior Scientist, Microbiome Science Resume Examples & Samples

  • Education & Experience: BS 7+ years’ experience, MS 5+ years’ experience, PhD 3+ years’ experience
  • Breadth of Technical Knowledge: Understands the application of domain skills and knowledge. Directs technical projects that may involve multi-disciplinary activities
  • Education & Experience: PhD in an area of microbiology, immunology, environmental health sciences, toxicology, cell biology, molecular genetics or related biological science with at least 5 years postdoctoral experience. Demonstrated ability to independently attract and execute R&D programs as evidenced by external funding and publication record
  • Technical Expertise: Ability to lead and conduct high-quality, productive research with responsibility for overall technical approach and execution in areas of importance to our NIH-, EPA- DOD- and/or DOE-sponsored programs
101

Senior Scientist, Microbiology Resume Examples & Samples

  • Technical Expertise: Technical expert. Selects and widely applies principles, theories and concepts in major field of specialization
  • Level of Responsibility: Fully competent scientist/engineer contributing to science and technology solutions in the conventional aspects of discipline specialty. PI or Co-PI on multiple or significant projects or tasks
  • Education & Experience: PhD in an area of microbiology, molecular biology, environmental sciences, cell biology, or other biological science with at least 5 years postdoctoral experience. Demonstrated ability to independently attract and execute R&D programs as evidenced by external funding and publication record
  • Technical Expertise: Ability to lead and conduct high-quality, productive research with responsibility for overall technical approach and execution in areas of importance to our DOE-sponsored programs and/or NIH-, EPA-, or DOD- programs
  • Level of Responsibility: Operates independently to design research strategies, responsible for meeting task scope, schedule and budget. The candidate will also be expected to develop and lead externally-funded research projects, and engage in client interactions and program reviews
102

Senior Scientist Resume Examples & Samples

  • Possess the ability to lead dynamic, multi-disciplinary teams of scientists and manage complex projects
  • Have a demonstrated record of strong leadership qualities, scientific talent, team building and motivation skills, and project management, as well as a proven commitment to the mentoring and development of junior scientific staff
  • Have obtained recognition via publications, awards, lecture invitations, or other honors
103

Senior Scientist Resume Examples & Samples

  • Develop engineering test study protocols, execute studies, perform data analysis and generate technical reports in support of targeted project milestones and goals
  • Research, develop and implement novel methods to address devices, mechanisms, equipment, or products that are not currently within the purview of existing industry or regulatory standards
  • Execute failure investigations
  • Manage small and large projects, ensuring that budgets and timelines are met
  • Publish at conferences and/or in peer-reviewed literature
  • Develop new skills and expertise
  • Assist in marketing individual and group skills to the scientific community and industry
  • Develop working relationships with others from internal practices, such as: Human Factors, Material Science, Polymers, and Electrical Engineering
  • Ph.D. in Mechanical Engineering or similar field
  • Emphasis in one of the following areas: Controls, Mechatronics, Mechanics, or Biomechanics
  • Experience with engineering related software, for example: LabView, Matlab, MathCAD, Solidworks, Autocad
  • Must be able to convey complex technical information and analysis to individuals both with and without technical backgrounds
  • Ability to work within project teams with strong desire to contribute, have potential for technical and project managerial leadership as well as desire to seek new client relationships
104

Senior Scientist Solid State Selection & Characterization Resume Examples & Samples

  • PhD Degree in Engineering or in Pharmaceutical Sciences, Chemistry (analytical/organic), Physics, or a related science
  • Experience and good knowledge in a number of the following areas: crystallization, solid state characterization techniques, form selection, salts and cocrystals, thermodynamic relationships between solid state forms, spectroscopy
  • You have good project management skills as well as communication skills (oral and written) allowing effective interactions
  • You are a team player, able to collaborate with different departments and with colleagues from the solid state selection group
  • You like to work in the lab
  • Fluent English (both spoken and written), willing to learn basics of Dutch language
105

Senior Scientist Ingredient Technology Resume Examples & Samples

  • Develop and execute work plans for key projects which may include bench-top formulation, sensory evaluation, consumer testing, pilot plant production, and product testing
  • Independently lead informal taste evaluations, summarize comments, conclusions, and next steps will little direction from manager
  • Mentor and supervise associate scientists across other ingredient categories and other projects
  • Proactively surface ideas and projects based on previous ingredient expertise
  • Develop new ingredient specifications and lead the internal review process for new ingredients or changes to current ingredients
  • Organize and facilitate supplier presentations to learn about potential new clean label ingredients and application in beverage systems
  • Proactively search for potential new clean label technologies with new suppliers
  • Evaluate new ingredients and alternate suppliers to identify potential cost savings opportunities
  • Develop and execute shelf life testing protocols for new ingredients
  • Troubleshoot ingredient quality issues based on experience
  • May travel up to 10% of time
106

Senior Scientist Resume Examples & Samples

  • Identify, pursue, plan, execute, and oversee all aspects of natural resource permitting, including direct and indirect coordination with stakeholders and jurisdictional local, state and federal agencies
  • Perform field investigations related to wetland delineations and threatened and endangered species habitat
  • Prepare biological assessments for threatened and endangered species
  • Perform environmental analyses in support of preparation of NEPA documentation
  • Assist in preparation of NEPA documentation
  • LI-RD
  • Bachelor's degree in Geology, Biology, Environmental Science, Engineering, Planning or related field plus 5-7 years of experience required
  • Master's degree in the Natural Sciences listed previously plus 3-5 years related experience preferred
  • Minimum of 10 years’ related experience, preferably within NEPA and/or Permitting practices preferred
107

Senior Scientist Resume Examples & Samples

  • Develop key relationships with relevant domestic and international authorities ultimately leading to joint development projects
  • Develop new surface modification for application in new products
  • Implement practical polymeric materials characterizations (adhesion, micelles, vesicles and aggregates, etc.)
  • Masters or PhD in polymer chemistry, polymer science, chemical engineering or organic chemistry
  • Master degrees with a minimum of 5 years of experience in R&D working in polymers synthesis and characterization
  • 5+ years of modern organic and polymer chemistry
  • 3+ years’ background in analytical chemistry
  • 5+ years of experience in polymers modification and characterization
  • 5+ years of expertise in polymeric materials characterization (solid and solution phase)
  • 3+ years of knowledge of various resin chemistries and waterborne polymers (modification with specific functionalities)
  • 5+ years of knowledge in surface modification of inorganic or organic substrates
  • PhD with a minimum of 3 years of experience in R&D working in polymers synthesis and characterization
  • Good understanding of membrane formation and membrane modification is desired
  • Understanding of chemical synthesis process optimization and scale up is desired
  • Experience with characterization techniques (GPC, DSC, DMA, TGA, SEM, AFM, NMR, UV-VIS, FT-IR, GC-MS, LC-MS, etc.) is highly desirable
  • Experience with D.O.E., process optimization and scale-up a plus
  • Experience in project management principles and practices is a plus
108

Senior Scientist Resume Examples & Samples

  • The generation and evaluation of detection systems for use in cancer diagnosis in manual and automated staining systems
  • To provide technical leadership to a project; develop, plan, and execute experiments to drive the development of detection systems, ensuring that delivery of the project to business is within budget and on schedule
  • Driving and supporting departmental innovations programmes and interacting with Innovations Department to initiative novel product development
  • To manage multiple internal stakeholders throughout the product development process, from tissue culture production to manufacturing, to quality control and quality assurance for the benefit of the project
  • Providing support to and deputise for the Head of Detection in regard to interdepartmental matters
  • Provide supervisory support and mentoring for a small project team
  • Ongoing awareness of competitor activity and new technologies
  • Significant experience of scientific techniques relevant to the role
  • Proven ability to write reports and supporting documentation to a high standard
109

Senior Scientist Resume Examples & Samples

  • Driving innovation, effectively lead research projects, and work in a highly cross-functional team of scientists and engineers
  • Develop an extensive knowledge-base and fundamental understanding of polymer-based adhesives, coatings, films, composites, blends, and membranes
  • · Develop novel membrane processing methods that can be scaled-up for high-yield manufacturing
  • · Work closely with development and product engineering groups to launch breakthrough products
  • · Experience with basic analysis tools, such as SEM, XRD, FTIR, DSC, TGA, and DLS
  • PhD or equivalent in (Chemical Engineering, Materials Science, Polymer Science, or Chemistry) with 1-3 years postdoctoral research and/or industrial R&D experience
  • MS or equivalent in (Chemical Engineering, Materials Science, Polymer Science, or Chemistry) with 5 years industrial / R&D experience
  • 1 to 3 years’ experience in characterization of films, adhesives, coatings, colloidal dispersions, and/or membranes
  • 1 to 3 years’ experience with processing methods for films, adhesives, coatings, and/or membranes
110

Senior Scientist Resume Examples & Samples

  • Lead one (1) active pharma collaboration, specifically for the feasibility, development and verification phases of assay development for a Companion Diagnostic Immunohistochemistry (IHC) or In Situ Hybridization (ISH) In Vitro Diagnostic assay
  • Serve as a primary point of contact for external pharma partner
  • Work closely with project management to ensure execution of project plans with an emphasis on On Time Delivery of project milestones and efficient team member utilization
  • Ensure own work and work of all R&D team members supporting assigned project is conducted in accordance with applicable protocols and work instructions and that all work is appropriately documented per procedure
  • Ensure assay development is consistent with FDA regulations and EU CE-IVD directives
  • Own the Design History File as defined per the Design Process procedure including but not limited to the Design and Development Plan, and Development and Verification Test Plans and Reports
  • Interpret results and document assay development with a high degree of complexity and scientific rigor and effectively organize documentation so that the process is traceable and clear
  • Oversees technical output of project team to ensure data quality
  • Promote collaboration and communication between R&D departments across the company
  • Support a culture of continuous process improvement and advise process improvement teams
  • At least 4+Years industry experience gained within an IVD development environment with increasing responsibility. Experience with IHC and ISH assay development is preferred
  • Experience working with quality and regulatory requirements under which diagnostic products are developed, commercialized and supported (i.e. FDA, EU CE-IVD )
  • Experience with FDA or EU CE-IVD quality requirements and the preparation of relevant documents for the submission of product information to these agencies
  • Strong experience in IVD Product Development, preferably with technical expertise in IHC, ISH assays on automated staining platforms
  • Demonstrable experience of providing guidance and mentorship within teams to drive the successful development and release of products through implementation and an ability to drive improvements
111

Senior Scientist Resume Examples & Samples

  • General laboratory responsibilities
  • Ability to manage complex technical projects
  • Ensure Central Testing Non conformances and CAPA’s are investigated and reported in a timely manner
  • Finding novel solutions to operational or technical problems using DBS
  • Management, coaching and mentoring of Central Testing Team members
  • Responsible for training and performance management of Central Testing Team members
  • Ensure Central Testing tasks are completed according to agreed timelines
  • Preparation, Performance and Documentation of Stability Study and QC Tests
  • Ensure Stability Studies are planned, managed and undertaken within set timelines
  • Writing Stability Study Plans, Reports and update of product shelf life
  • Experience in performing routine and relevant QC / Stability Study laboratory techniques (microtomy, cryotomy, immunohistochemistry procedures including pre-treatments, automated stainers and slide screening), standards, systems and operate equipment in alignment with relevant regulatory standards would be beneficial but not essential
  • Proficient in using laboratory equipment, e.g. pH meters, balances, micropipettes, autoclave, etc
  • Support other site project activities, when required, outside of Central Testing
  • Experience of project management
  • Experience of people management
  • Proven and demonstrable experience in writing study plans and reports
  • Histology or immunohistochemistry experience including microtomy and slide screening
112

Senior Scientist Resume Examples & Samples

  • Write validation/qualification protocols and data summaries. Strong writing skills are required for this position
  • Collects and analyzes scientific data. Position may involve some laboratory work
  • Work with cross-functional teams to solve complex technical issues
  • Implements process improvements and develops specifications, conducts process validations
  • Facilitates technical meetings and provides technical training to manufacturing personnel
  • Manages and facilitates project meetings
  • Bachelor's Degree (chemistry, engineering or biology related) with a minimum of 5 years’ experience
  • Excellent communication skills (both written and oral) are a must
  • Effective interpersonal skills
  • Knowledge of MicroScan consumables and instruments a plus
  • Experience with manufacturing processes a plus
  • Experience with validation,
  • Experience with risk management
  • Knowledge of FDA and ISO standards
  • Bachelor’s degree in field with 5+ years experience OR
  • Master’s degree in field with 3+ years experience OR
  • Doctoral degree in field with 0-2 years experience
113

Senior Scientist Resume Examples & Samples

  • Support development of robust formulations and processes through optimization, scale-up and validation work applying QbD principles incl. risk assessments and DoEs
  • Communicate and address problems, perform safety and literature searches under guidance from more experienced team members
  • Awareness for safe handling of chemicals, potentially dangerous materials and equipment. English
  • Adequate scientific or technical knowledge in a specific area (e.g. Emulsions, Emulgels or liquid parenteral and freeze dried products)
  • Basic knowledge in scientific/technical areas of collaboration
114

Senior Scientist Mass Spectrometry Resume Examples & Samples

  • Perform profiling and characterization of therapeutic proteins, protein-conjugates, and their posttranslational modifications by MS using state-of-the-art LC-MS equipment
  • Compile analytical data from different analytical methods, write technical reports, and present conclusions in expert team meetings
  • Develop new methodologies and improve processes for effective characterization of biotherapeutics as well as automated data analysis
  • Ensure maintenance of specialized technical equipment and organization of the general lab infrastructure
  • Effectively manage analytics characterization timelines to support several projects in parallel, and work closely with other teams in an international setting
  • Provide technical training to team members as required
115

Senior Scientist Drug Substance Development Resume Examples & Samples

  • Design, plan, supervise and monitor all activities of assigned units/projects. Interpret results, evaluate data, draw relevant conclusions and write reports, lead and coordinate local scientific team(s)
  • Lead, manage and support the technical drug substance sub-team with regard to late stage development processes through clinical and commercial drug substance (DS) supply (incl. process characterization, validation, regulatory filings, and technology transfers)
  • Contribute to decision making that impacts goals, objectives and strategies
  • Actively contribute to resource allocation/outsourcing strategies; communicate and escalate potential risks with department and project management
  • Generate scientific documents to hand over to internal and/or external partners (e.g., manufacturing, authorities, external companies) and support generation of international registration documents
  • Monitor the preparation and timely availability of all relevant technical source documents necessary for regulatory filings and health authority responses and provide strategic review of relevant CMC documents
  • Evaluate, develop and implement new technologies
  • Report and present scientific/technical results internally and publish/present externally in scientific journals and conferences including patents
116

Senior Scientist, Raw Materials Resume Examples & Samples

  • Works closely with Manufacturing clients to develop individual raw material control strategies
  • Defines risk tolerance and risk strategies for the raw materials supply and release program for the Manufacturing programs at the Philadelphia location
  • Takes a leadership role in defining appropriate test methods/testing strategy for raw materials
  • Evaluates and defines whether client raw materials are appropriate for the clinical phase of the biological product
  • Serves as a key member of the Material Review Board (MRB)
  • Works closely with Supply Chain and the MRB to review supplier change notifications and other items related to raw materials
  • Assures all activities in the area of raw materials meet cGMPs, FDA and International regulatory requirements
  • Prepare, own and revise SOPs relevant to the site raw material control strategy
  • Participates in PAIs, regulatory and quality audits, as needed
  • Participates, as needed, in evaluating supplier quality including vendor site visits
  • Assists, as needed, in writing CMC sections for raw materials
  • Develop and qualify assays for the release testing program when needed
  • B.S. in a Chemistry, Biological or Material Science program plus a minimum of 7 years experience, M.S. or Ph.D. with a minimum of 5 years experience in pharmaceutical organizations preferably in a quality, regulatory, or QC role related to raw material release
  • Thorough knowledge and experience with GMP a must. Strong knowledge of USP, FDA regulatory guidance documents, EU regulations and ICH guidelines
  • Working knowledge of regulatory and quality raw material requirements for Phase 1 through post approval, including the associated change management and reporting
  • Familiarity with US and EU regulations for Cell and Gene Therapy products and raw materials
  • Strong oral and written communication skills. Strong organizational skills with the ability to multi-task and prioritize assignments. Ability to write reports, meeting agendas/minutes, business correspondence, and procedures such as SOPs
  • Ability to effectively manage multiple projects under short time lines
  • Ability to work under pressure and effectively lead in a fast-paced, dynamic technical environment
  • Working knowledge of Microsoft suite of software products including Excel, Word and PowerPoint
117

Senior Scientist Resume Examples & Samples

  • Ph. D. Degree in Chemistry, Chemical Engineering, Biology - or a similar field
  • 3 year or more experience in developing products for the biopharmaceutical, protein analysis or life science market. Experience with Bio-layer Interferometry (BLI), Surface Plasmon Resonance (SPR) or similar label-free technologies preferred
  • Has expertise in chemical modification of silica and related inorganic surfaces, including self-assembled monolayers
  • Experience characterizing surfaces using surface analysis techniques such as ellipsometry, XPS and fluorescence preferred
  • Fluent in English Language Oral and Written Skills
  • Good Communication Skills and strong in technical writing and presentation
  • Problem Solving Skills
  • Ability to Work in Team Environment
118

Senior Scientist Resume Examples & Samples

  • Plan and execute experimental designs to optimize the organoleptic, nutrient, microbiological and physical quality of new products while adhering to the relevant internal and external constraints
  • Evaluate test results and develop conclusions and action plans, and then communicate those recommendations through written reports and verbal updates
  • Develop ingredient, formula and process specifications to ensure product quality, safety and consistency during commercial manufacture
  • Interact with cross-functional business teams including marketing, operations, quality, purchasing, regulatory and legal
  • Develop and manage a project plan and corresponding budget
  • Manage and mentor junior scientist/s
  • PhD in Food Science or related scientific field with 3-7 years of relevant experience; MS in Food Science or related scientific field with 7 – 15 years of experience or BS in Food Science with 11 – 20 years relevant experience
  • Knowledge of formulation, processing and packaging aspects pertaining to liquid and powder forms
  • Intermediate computer and math skills required
  • Experience with spreadsheets (Microsoft Excel) and statistical designs of experiments is preferred
119

Senior Scientist Technical Support Resume Examples & Samples

  • Technical Support - Assist in resolution of multiple complex technical and quality issues across ADD Sites; TPMs and or functions (instrument; reagents; software and commodities). Anticipate; recognize and resolve technical issues
  • Sharing Knowledge - Presents complex technical information to internal and external groups. Shares scientific information and expertise with customers and regulatory agencies. Experience mentoring and teaching others to facilitate timely resolution of product and process technical issues
  • Strategic and Results Orientation - Demonstrates fiscal responsibility through actionable recommendations and accomplishments. Translates top-level goals to specific goals and aligns activities with respective strategic business priorities
  • 4 years’ related work experience. Advanced degree preferred. (Advanced degree(s) may offset required years of experience)
120

Senior Scientist Resume Examples & Samples

  • Applies quantitative methods: analyzes data; evaluates results; forms conclusions; and provides/implements process or document improvements
  • Integrates data from multiple sources and identifies critical process variables
  • Evaluates data using various appropriate analytical and statistical methodologies to achieve results
  • Summarizes data and analyzes results; independently formulates conclusions; and determines future experiments
  • Independently designs and executes a series of experiments to test hypotheses related to project outcomes
  • Utilizes DOE where appropriate
  • May assist in the design of experiments for others
  • Determines priorities for experiments
  • Applies advance scientific knowledge to projects
  • Recognizes and resolves technical problems
  • Prepares results of projects internally and may present externally
  • Produces reports and documents utilizing advanced writing skills
  • Reviews; evaluates; and critiques presentations for others
  • Presents complex technical data to large and diverse groups
  • Demonstrated success
  • Outstanding verbal, written, and documentation skills
  • Excellent collaboration and interpersonal skills
  • Able to manage multiple tasks and priorities simultaneously and to adapt to changes in program priorities
  • Seeks out; uses; and builds upon ideas from others
  • Builds relationships by helping others feel valued and by working as a team to achieve mutual goals
  • Minimum of 2 years related work experience, preferably in IVD or biotechnology industry
  • Experience with statistical software i.e. advanced Microsoft Excel skills, JMP, SAS, Tableau, is preferred
  • Knowledge of regulations and standards affecting IVDs and Biologics
121

Senior Scientist Resume Examples & Samples

  • Responsibilities include working with multiple project teams to coordinate logistics and to conduct in vivo studies
  • Conduct studies within timelines to help achieve milestone decisions; anticipate potential hurdles, and identify alternative strategies to minimize impact to project goals
  • Maintain accurate and timely records of research, and develop and deliver scientific presentations and reports for internal meetings
  • Work as part of a highly collaborative interdisciplinary team in an integrated and well-supported research laboratory
  • Reviews, comprehends and complies with all SOP’s and quality assurance standard pertaining to specific area
  • Strong in vivo skills, significant experience with subcutaneous and orthotopic mouse tumor models, including cell inoculations, tumor measurements, and multiple dosing routes
  • As this position is part of a dynamic matrixed organization, excellent oral and written communication skills are essential
  • The ideal candidate has proficiency in a wide range of in vivo and ex vivo techniques and a willingness to adopt new skills as needed
  • Competency with software programs, including MS Excel, Powerpoint, Word
  • Background in immuno-oncology research
  • Experience with in vitro mammalian cell culture
  • Proficiency with the software programs Prism and Study Director
  • Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance
  • Learns fast, grasps the "essence" and can change course quickly where indicated
  • Creates a learning environment, open to suggestions and experimentation for improvement
  • Embraces the ideas of others, nurtures innovation and manages innovation to reality
122

Senior Scientist, Cell & Molecular Biology Resume Examples & Samples

  • Become a subject matter expert on Hybridoma generation (including immunization technologies)
  • Lead Hybridoma generation campaigns from designing immunization strategy and screening funnel to all phases of Hybridoma generation including cell culture and fusion, antibody screening, characterization and production
  • Optimize Hybridoma generation workflow
  • Explore and develop innovative solutions with hands-on laboratory work and literature review to support novel biologics generation
  • Impact projects through both experimental design and lab activities
  • Generate panels of characterized monoclonal antibodies using Hybridoma technique
  • Deliver reliable and reproducible data in a timely manner
  • Conceive and implement novel experimental approaches to answer scientific questions
  • Demonstrate experimental precision and data analysis skills
  • Investigate, identify, develop, and optimize new methods/techniques with hands-on laboratory work and literature review
  • Develop productive collaborations and communication with other groups, across therapeutic areas
  • Demonstrate scientific excellence, work ethic, and dedication to team/project goals
  • Plan, lead and execute successful Hybridoma campaigns from choosing immunization strategy and developing screening funnels to generation and characterization of monoclonal antibodies
  • Conduct all phases of Hybridoma generation including cell culture and fusion, antibody screening, characterization and production
  • Perform laboratory research competently and independently
  • Analyze and interpret results, noting significant deviations
  • Report findings at team meetings
  • Learn and develop new techniques
  • Place data in proper scientific context by reviewing relevant literature
  • Demonstrate proficiency in multiple experimental techniques and ability to appropriately modify protocols to suit the changing needs of research
  • The ideal candidate is expected to work on multiple projects in a team environment
  • PhD and 3+ years of experience
  • Experience in Immunology
  • Proficient in cell culture
  • Knowledge immunoassays including ELISA and flow cytometry
  • Hybridoma generation
  • VH and VL sequencing and molecular cloning experience is a plus
  • Experience with automated laboratory processes and programming
  • Antibody purification and characterization
123

Senior Scientist, Cell Culture Resume Examples & Samples

  • Develop and characterize highly-productive CHO cell culture processes suitable for cGMP biotherapeutic manufacturing within project timelines
  • Develop methods
  • Maintain a high level of productivity in the lab, with clear and accurate documentation
  • Work collaboratively and cross-functionally on multiple projects with colleagues in Process Sciences, Manufacturing Sciences, Biologics/Discovery and others to meet team and company goals
  • Proactively seek out new information and opportunities to advance our technologies and pipeline
  • Critically evaluate relevant scientific, regulatory and business advances and integrate this knowledge
  • Contribute to the smooth and effective operation of the cell culture process development labs
  • Effectively present scientific data and concepts to internal and external audiences
  • Author and review technical reports, protocols and other key documents
  • Understand and adhere to corporate standards regarding code of conduct, documentation, safety, appropriate handling of materials, and GxP compliance
  • Ph.D. in biological sciences, chemical engineering or related discipline with 0-3 years of relevant experience in the biopharmaceutical industry (or BS/MS degree with at least 6 years relevant experience)
  • Thorough practical and theoretical understanding of cell culture process development to enable cGMP biotherapeutics manufacturing and associated areas of expertise (e.g., cell and molecular biology, process development, process scale up and scale down, recombinant protein production, protein characterization)
  • Strong scientific curiosity with a passion for problem-solving and optimization
  • Self-motivated with excellent attention to detail and ability to multi-task
  • Strong organizational, planning and trouble-shooting skills
  • Skilled in using common software packages such as Microsoft Office 2010
  • Expertise in media development, high-throughput cell culture and screening technologies, bioreactor operations, and statistical data analysis tools are highly desirable
124

Senior Scientist Resume Examples & Samples

  • Develop and optimize new strategies to process cellular and tissue samples for proteomics analysis
  • Active contributor on developing new chemical biology tools and knowledge
  • Integrate data sets generated from multiple data sources to strengthen research hypotheses
  • Interact with the broader scientific community to bring new technologies to the group and make recommendations on their utility
  • Regularly present and publish work in high level journals and conferences
125

Senior Scientist, Synthetic Organic Chemistry Resume Examples & Samples

  • Demonstrate the ability to resolve key project hurdles and assumptions by effectively utilizing available information and technical expertise
  • Proactively seek out new information in the literature and incorporate this into individual project(s) as well as the overall program
  • Effective writer and communicator of research or other regulatory materials
  • Publish project-related research in high-impact factor peer-reviewed journals, R&D reports, patent applications and/or regulatory documents/filings
  • Participate in establishing project goals, defining short and long-term scientific strategies, and contribute to the generation of project-related documents and presentations
  • Use external information to gain competitive intelligence. Act as advocate to integrate this knowledge into the group's research efforts
  • Collaborate with functional and technical experts to facilitate scientific achievement
  • Keep accurate and current records of research and/or project related activities according to AbbVie policies
  • May supervise one or more direct reports and proactively engage in their development
126

Senior Scientist Resume Examples & Samples

  • The successful candidate will be part of a research group that will study the mechanistic interactions of anti-TNF biologics with various cells within the context of diseased tissues primarily in skin
  • The goal of the studies will be to shed light on observed clinical results
  • The ideal candidate should be a critical scientific thinker and problem solver
  • The candidate is expected to have a very good knowledge of the therapeutic antibody field and basic antibody characteristics and functions
  • PhD in immunology/cell biology or related field preferably with some experience in research in the environment of a pharmaceutical or Biotech company
  • The successful candidate will have a strong record of scientific accomplishment as demonstrated by a publication record and a proven ability to work productively and creatively in a multi-disciplinary environment
  • Proficiency in standard cell biology, immunology and biochemistry techniques such as human leukocyte and tissue preparation, tissue culture, in vitro and ex vivo bioassays is required
  • Prior experience with auotoimmune disease models, including dermatological diseases, rheumatoid arthritis, biomarker work, immunohistochemistry, image analysis as well as functional antibody characterization such as BIAcore, ELISA and FACS assays and biologics mechanism of action studies is highly desirable
  • Strong interpersonal and excellent written and verbal communication skills are essential
127

Senior Scientist, Flow Cytometry Resume Examples & Samples

  • Manage the flow cytometry group including a newly established CyTOF capability
  • Provide advice and guidance to teams requiring flow cytometry support
  • Participate in preclinical and translational research through the application of flow cytometry
  • Design and develop biomarker assays for transfer to CROs
  • PhD in immunology or related field and 6+ years of flow cytometry experience related to immunology. Pharmaceutical industry experience preferred
  • Extensive knowledge and experience with flow cytometry; ability to design and execute strategies to meet the needs of project teams; experience with CyTOF desired
  • Experience developing biomarker assays to enable projects to transition to the clinic; experience working with CROs to enable clinical trials desired
  • Ability to integrate information from multiple disciplines to advance projects
  • Demonstrated ability to manage a team
  • Excellent interpersonal, leadership & organizational skills with a demonstrated ability to work collaboratively with scientists from multiple disciplines to advance drug development
128

Senior Scientist Resume Examples & Samples

  • Lead cross-functional efforts to develop optimal strategies and to address specific toxicology issues
  • Contribute and author regulatory filing documents and correspondences
  • Represent preclinical safety at external regulatory meetings
  • Effectively communicate and develop relationships cross functionally within AbbVie-Redwood City, PCS organization, Development Sciences organization, and the project teams
  • Quarterly travel to Lake County, IL to maintain strong collaborations and knowledge of the Preclinical Safety organization
  • PhD in biological sciences or related field
129

Senior Scientist, Exploratory Oncology Resume Examples & Samples

  • Conceive, execute and champion novel target validation strategies in the field of Oncology
  • Champion novel functional genomic/cell based screening and target identification approaches and technologies
  • Develop and maintain appropriate in vitro assays; in vivo/ex vivo analyses of tumor cell populations
  • Contribute substantially to team research strategies
130

Senior Scientist, Cell Line Development Resume Examples & Samples

  • Oversee the development of mammalian cell lines, especially CHO cells, for production of biologic therapeutics
  • Serve as Subject Matter Expert on Project Teams for early and late-stage projects. Author and review documents in support of regulatory filings
  • Routinely demonstrate scientific initiative and creativity in research or development activitiesHighly autonomous and productive in performing laboratory research or method development, requiring only minimal direction from or interaction with supervisor
  • Demonstrates high proficiency across a wide range of relevant technologies a high level of productivity in the lab and/or pilot plant
131

Senior Scientist, Genetics Research Resume Examples & Samples

  • Conduct statistical genetic analyses to determine genotype-phenotype relationships including mixed model regression, linear and logistic regression, rare variant aggregate tests, and family-based tests for quantitative biomarkers and disease traits
  • Independently translate and implement algorithms and protocols in a high performance computing environment
  • Optimize existing pipelines and review current workflows, as well as contribute to the establishing new pipelines, workflows, and underlying methodology
  • The ideal candidates will have a high degree of statistical and mathematical competency with experience applying these skills to human statistical genetics problems (e.g. demonstrated with relevant publications)
  • Strong communication skills are essential as well as fluency in one or more or relevant programming languages, such as R, Python, Java, or C++
  • Experience with cloud computing, version control, and Docker or similar technologies
  • Familiarity standard tools and data formats related to genetic data, such as those encountered when analyzing high-throughput whole exome or whole genome data, such as GATK, (g)VCF, CRAM, BAM, FASTQ
132

Senior Scientist, Human Genetics Resume Examples & Samples

  • Devise and execute studies to determine genotype-phenotype relationships from large, human sequencing databases; work with computational biologists and others to develop and provide analytical support for mining and interpreting NGS and array data across multiple projects
  • Provide biological interpretation for genetic, genomic and epigenetic associations derived from large scale human genetic sequencing databases
  • Collaborate with Functional Genomics Group to design and execute studies to provide mechanistic understanding for genotype-phenotype relationships
  • Collaborate with scientists across different Early Discovery therapeutic areas to interpret and incorporate genetic findings into new targets or for validation of existing targets
  • Provide support for external collaborations and consortia involving human genetics
  • PhD in Human Genetics, Molecular Genetics, or closely related field, with expertise in genetic association studies, rare disease analysis, and/or family based genetic studies
  • The ideal candidate should have strong background in genetic association studies, rare disease analysis, and family based genetic studies
  • Candidates should have demonstrated ability to design and lead human genetics studies delivering novel genetic findings and medically relevant gene discoveries
  • Experience working with large human genetic sequencing databases
  • Experience interpreting family-based and rare disease genetic studies
  • Experience with large-scale research projects involving next generation DNA sequencing data (e.g. whole exome and whole genome) as well as array based genotype data
133

Senior Scientist, Immune Oncology Resume Examples & Samples

  • Conceive and execute experimental strategies in the field of immuno-oncology to support biologic drug discovery with a high level of experimental vigor and quality
  • Have extensive laboratory research experience and a desire to continue in a laboratory-focused role
  • Able to prioritize and manage multiple research activities and possess a broad range of technical expertise and knowledge in biologics and immune oncology that includes innate immune response by macrophages, NK cells, MDSCs; and adaptive immune response by antigen presenting cells, helper T cells, regulatory T cells, and cytotoxic T cells
  • Contribute substantially to team research strategies, and communicate results to multi-disciplinary teams
  • Position will be filled at level commensurate with extent of education, experience, and accomplishment
134

Senior Scientist Resume Examples & Samples

  • Coordination and implementation of studies and management of projects with respect to in vitro evaluation and characterization of PET radiotracers and drug candidates (hands–on involvement in the lab working with in vitro and ex-vivo techniques)
  • Provide the imaging team with scientific and technical input in order to improve study design, interpretation of results, reporting and communication
  • Utilize appropriate computer software packages effectively to support the analysis and interpretation of study data
  • Maintain and expand critical expertise within the field of pharmacology as it relates to imaging and relevant platform technologies across therapeutic areas, diseases and methodologies
  • Design and perform experiments aimed at the characterization of novel PET tracers/ligands in collaboration with chemistry and image analysis teams
  • Scientific quality and review of study protocols used in support of pre-clinical and clinical studies
  • Input into the analysis and interpretation of PET data, independently or in conjunction with other experts within the imaging team
  • Manage projects with respect to the evaluation and characterization of radioligands carried out within AbbVie and through collaboration with selected external sites
  • Training colleagues in in vitro/ex vivo techniques related to imaging
  • Demonstrated record of scientific achievement in peer reviewed journals
  • Demonstrated understanding and application of key pharmacological in vitro techniques for characterization of novel compounds and/or biological targets
135

Senior Scientist Resume Examples & Samples

  • Design and execute/conduct in vivo studies (syngeneic and humanized mouse models, as well as GEMMs) aimed at drug discovery in the immuno-oncology space
  • Use detailed knowledge of state-of-the-art tools and approaches to enhance in vivo evaluation of novel therapeutics and/or identify new targets
  • Execute secondary cell-based assays across various technology platforms (e.g. FACS, cell sorting, etc.)
  • Perform supporting assays (immunophenotyping, cytokine profiling, ELISA and/or western blot analysis of tissue lysates) to assess target modulation levels and downstream effects
  • Participate in oncology target identification and validation
  • Demonstrate a high level of initiative in troubleshooting experiments and performing data analysis
  • Effectively collaborate across cross functional teams
  • Present research findings to project teams and governance bodies and prepare technical reports
  • Work with external academic, biotechnology, and contract research organizations to advance our understanding of oncology diseases
  • Mentor and guide other scientists in the group. May have direct report(s) depending upon managerial experience
136

Senior Scientist Resume Examples & Samples

  • Lead analytical characterization and assessment of development samples and clinical trial supplies (e.g. GMP compliant stability and release testing)
  • Lead activities associated with formulation design and characterization for new biologic compounds
  • Lead small project team in the execution and design experiments for method development and validation studies
  • Author and/or review key regulatory documents, laboratory data, technical memos and reports
  • Mentor junior staff in troubleshooting of equipment and experimental problems
  • Encourage ideas for continuous improvement activities and initiatives within work group
  • Understand and adhere to corporate standards regarding code of conduct, safety, and GXP compliance
137

Senior Scientist Resume Examples & Samples

  • PhD in biochemistry, biology, immunology or a related discipline
  • 4-6 years of bench experience working with antibodies, immunoassays, flow cytometry and chemical conjugations
  • Develop high-quality, robust antibodies and multiplex immunoassay kits with associated documentation
  • Identify and employ new technologies for antibody and assay development
  • Independently design, plan and conduct laboratory experiments in support of new product development
  • Identify and resolve problems in experimental design
  • Maintain good laboratory records and presentation of regular internal research reports
  • Provide clear manufacturing instructions, QC specifications and technical support to Manufacturing for developed products including details of performance, stability and packaging
  • Prepare technical reports, product summaries, protocols and SOPs, quantitative analyses and journal publications, where appropriate
  • Presentation to a wider audience may be necessary which includes attendance at conferences to communicate available products, research data generated and acquire new product and collaboration leads
  • Provide technical assistance and marketing support to the commercial operations selling reagents, antibodies, and immunoassay kits
  • Provide technical assistance to customer support and directly to customers for reagents, antibodies, and immunoassay kits
  • Comply with all safety and quality regulations
  • Routine maintenance and troubleshooting of scientific equipment
  • May be required to supervise junior members of staff
  • May be required to perform other duties as required/assigned
  • PhD in biology, immunology, biochemistry or related subject
  • Prior hands on development and optimization of antibodies and single/multiplex immunoassays
  • Prior hands on experience in antibody applications including flow cytometry, immunofluorescence microscopy, Western blotting, ELISA and antibody conjugations
  • A detailed understanding of the biology and chemistry of immunoassays
  • A detailed understanding of the biological pathways involved
  • Cell culture and specimen handling experience
  • Demonstrated ability to work independently, and in method development, experimental design, and data analysis
  • Previous experience supervising technical staff
  • Knowledge of GLP PhD with 3+ years’ experience in an antibody or assay development environment is highly desirable. Prior experience in Life Sciences reagents industry very highly desirable. and GMP a plus
  • Critical thinking and independent judgment with only general direction necessary
  • Excellent computer skills including instrumentation specific software, and proficiency in Microsoft office
  • Sitting, using a computer
138

Stability Senior Scientist Resume Examples & Samples

  • Design and lead development & registration phase stability studies for API and /or Drug product development programs
  • Support preparation of Client Proposal for stability aspects and strategies
  • Participate in projects as stability expert
  • Provide authorship of stability protocols and reports for complex stability studies
  • Act as the main technical point of contact for given Clients portfolio for Stability projects
  • Ensure that all the stability work carried out is performed in compliance with study protocols
  • Prepare for inspections and audits as appropriate and act as spokesperson if applicable for stability related topics
  • Work with other Team Members to share key learning and best practices
  • Coach and grow more junior matrix team members
  • Degree on Chemistry & Pharmaceutical Technology or equivalent scientific subject highly desirable as well a Master in Regulatory Sciences
  • At least 10 year industrial experience in Pharma GMP analytical labs and/or in CMC Regulatory Groups in preparation of IMPD/IND
  • In depth understanding of ICH Quality Guidelines (especially stability, impurities and specification ones) and know-how of EU/US CMC Regulatory Documentation and of International key Stability Guidelines in a project application perspective
  • Established experience in designing R&D stability studies, preferably within Phase I to IIb projects up to Registration, with ability to build suitable stability strategies to support submissions
  • Good understanding of the analytical requirements for drug substance and drug product development programs (both technically and from a regulatory point of view)
  • Practical and/or good theoretical knowledge of analytical chemistry techniques such as chromatography (especially HPLC), dissolution, spectrometry
  • Knowledge of GLP/GMP requirements, including technical and regulatory requirements related to GMP
  • Excellent team working ability
  • Ability to manage activities with tight deadlines and high matrix complexity
  • Ability to complete assigned work and progress against expectations to ensure customer needs are satisfied
  • Excellent ability to write and/or review scientific and technical reports
  • Ability to give written/oral updates/presentations
  • Be effective and efficient in the use of time to achieve work related goals
  • Good knowledge of spoken English language and excellent as written
139

Senior Scientist Resume Examples & Samples

  • Oversee the development and validation of analytical methods for drug substances and drug products
  • Conduct/manage routine and advanced analytical tests in accordance with SOPs and regulatory guidance
  • Write and or review protocols, reports, methods, standard operation procedure, and submission documents
  • Perform independent scheduling and coordination of analytical activities
  • Analyze analytical data, identify trends, and provide recommendations
  • Troubleshoot analytical problems and conduct laboratory investigation and prepare laboratory investigation report
  • Proactively provide suggestions on how to improve methods, lab practicees or lab systems
  • Review and evaluate drug substance supplier’s technical documents and provide recommendation in API vendor selection
140

Senior Scientist Resume Examples & Samples

  • Develop formulation presentations for first-in-human clinical trials, as well as, Phase 2 through Ph3 studies
  • Support cGMP manufacturing at our CMOs (includes review of batch records, specifications, deviations etc.)
  • Support technical transfer of drug product manufacturing for agents in all stages of clinical development, including Validation and Launch
  • Execute experiments per the project plans in-house based on capability and capacity or through an outsourced capacity
  • Write experimental protocols and study plans with reports documenting the results
  • Independently lead projects from drug product development point of view with minimal supervision, identify risks and propose mitigation strategies
  • Represent the Pharmaceutical Chemistry Section in CMC team meetings
  • Provide guidance to colleagues in research to formulate advanced leads for in vivo testing
141

Senior Scientist, Pre-clinical Resume Examples & Samples

  • Write and edit preclinical study reports
  • Write preclinical sections for preclinical submissions
  • Work closely with other functional areas and colleagues to insure that all studies are performed in a quality, timely and scientific manner
  • Collaborate with project team members on development strategy
  • Develop safety-related issue mitigation or resolution plans and coordinate execution of the experimental plan as required
  • Prepare and edit non-clinical documents for regulatory submission (e.g. IBs, and regulatory briefing documents)
  • The Scientist will report directly to the Executive Director, Preclinical Development
  • Ph.D. in Biological Sciences, Toxicology, Pharmacology, DVM or M.D required
  • 6-8 years drug development experience, with minimum 3 years working in industrial pharmaceutical toxicology/safety assessment drug development
  • Ability to synthesize and interpret diverse, multidisciplinary data sets
  • Extensive knowledge/understanding of pharmacology pathways and MoAs relating to the IND-enablement of biologic programs with preference given to gene therapy programs
  • The ability to work independently and to collaborate with a multi-disciplined group in a goal- and team- oriented setting is required
142

Senior Scientist, Neuropharmacology Resume Examples & Samples

  • A proven track record in progressing drug targets from validation to early clinical development is an asset
  • A strong and established scientific background in invitro and/or in vivo pharmacology with a demonstrated track record of independent research and peer-reviewed publications
  • Experience in conducting in vivo models of disease and evaluating pharmacological interventions is preferred
  • A thorough understanding of PK/PD relationships is highly desirable as is experience conducting surgical recovery models in rodents
  • Comfortable with changing direction and taking risks
  • Develop in vitro and in vivo innovative approaches and technologies to identifying mediators of neuromuscular and neurodegenerative diseases and to validate novel therapeutic targets
  • Lead cross functional drug development teams to bring therapeutic candidates in to clinical development
  • Provide strategic input into the identification and validation of novel targets that complement the neuropharmacology portfolio
  • Develop a creative and innovative research plan
  • Provide scientific oversight and career development opportunities to Ph.D./MA/BA scientists with broad scientific backgrounds
  • Develop collaborative relationships with key opinion leaders
  • Establish and maintain scientific eminence amongst the academic community by publishing and presenting research at internationally-recognized scientific conferences
143

Senior Scientist Resume Examples & Samples

  • Interact with cross functional matrix team personnel within BioMarin and contribute to strategic and scientific planning and execution
  • Accountable for developing and implementing translational strategy with a focus on clinical dose , route and regimen selection
  • Analyze and interpret PK/PD data from nonclinical and clinical studies using appropriate quantitative methodologies
  • Interact with external collaborators, key opinion leaders and vendors as appropriate
  • Author study reports, sections to INDs, NDAs, etc. and publish findings at the appropriate time
  • Serve as a mentor to junior scientists and contribute to process improvement with an eye towards efficiency and consistency
  • Be the clinical pharmacology representative on cross functional initiatives and on due diligence teams upon management request
144

Senior Scientist, Process Research Resume Examples & Samples

  • Acquire knowledge of and assist in implementing new technologies; Ensure integration of new technologies and department initiatives into daily work to enhance productivity
  • Effectively communicate own and/or team’s work and deliver project updates to senior level management clearly in oral and written forms in the context of project goals
  • Responsible for lab/group operation including coaching, mentoring, training, supervising and developing staff when assigned; Participate in recruiting when needed
  • Develop and maintain visibility through presentations and publications; Take the lead in publications and patents when needed
145

Senior Scientist, Medchem Resume Examples & Samples

  • Proposes, justifies, and carries out new assays, methods, procedures, technology, and/or automated systems that improve group efficiency and effectiveness
  • Solves assay and technical/automation problems and achieves productivity guidelines
  • Understands assay related science and technology or automated systems as they relate to the drug discovery process
  • Interprets results, efficiently troubleshoots assays and processes or automated systems, and writes protocols for new and transferred assays or automated processes
  • Able to take responsibility for development, productivity and compliance of associate
  • Oversees efficient laboratory operation and performs BMSG and department related activities
  • Effectively presents and defends own and HTB’s work in project and departmental context; Publishes papers and presents at external scientific meetings
  • Complies with all required company, R&D, and departmental guidelines, policies, procedures, and training; Performs all work in a safe manner & maintains a safe laboratory environment
146

Senior Scientist, Process Chemistry Resume Examples & Samples

  • Independently propose, direct and perform scientific experiments with a predefined project goal including developing new methodologies, protocols and procedures; Keep abreast of relevant literature and maintain a high level of expertise in own field; Protect intellectual properties through new patent applications
  • Develop an understanding of R&D team goals and work effectively toward achieving them in a multidisciplinary team environment; Either assumes departmental responsibility for projects when assigned or demonstrate leadership initiative in technical expertise areas to advance projects towards key milestones, as per requirement
  • Contribute to departmental administration when needed; Demonstrate fiscal responsibility with respect to cost of experiments, technologies, external collaborations, and travel
  • Comply with all regulations and policies; Perform all work in a safe manner; Maintain proper records (notebooks, batch sheets, etc.) per relevant SOPs
147

Senior Scientist Resume Examples & Samples

  • Develops an understanding of R&D team goals and works effectively toward achieving them; Either assumes departmental responsibility for projects when necessary OR has ability to participate as representative on multiple project teams and contribute to defining expertise-related aspects of overall program goals
  • Prepares clear technical reports, publications and oral presentations. Independently communicate results in the form of reports and or presentations; Presents responsibly and defends own work at meetings; May deliver updates to senior level management in context of overall project goals
  • Complies with all applicable regulations; Ensures that work performed in area of responsibility is conducted in a safe and compliant manner; Maintains proper records in accordance with SOPs and policies
148

Senior Scientist Resume Examples & Samples

  • Ph.D. Degree or equivalent experience in protein mass spectrometry
  • Well-qualified candidates will have 2-5 years’ experience in this area including antibody characterization
  • Strong inter-personal skills are required as are excellent oral and written communication abilities
  • Other desirable attributes include superior problem solving skills, strong motivation and high levels of organization
  • Thorough understanding of early biologic drug discovery
  • Demonstrated ability to generate novel ideas and concepts
  • Ability to communicate effectively both orally and in writing in an inter disciplinary environment
149

Senior Scientist, Medchem Resume Examples & Samples

  • As member of an interdisciplinary team of biologists, medicinal chemists, crystallographers, biophysicists, and drug discovery support scientists contribute to the advancement of drug discovery projects by providing state of the art computer-aided drug design input
  • Participate in technology initiatives, and be directly engaged in the development of tools that improve computational chemistry approaches and workflows for structure-based and ligand-based drug design and cheminformatic analyses
  • Participate in the evaluation of CADD software
  • Maintain all appropriate notebook records of all studies and satisfy all normal lab SOP requirements
  • Report to the CADD Supervisor
150

Senior Scientist Resume Examples & Samples

  • Enable and provide experimental structural input and support that drives NCE projects to achieve milestone goals
  • Strong technical skills in protein crystallization and protein crystallography
  • Experience in preparing and characterizing protein samples for crystallization
  • Demonstrated expertise in the design and implementation of crystallization trials
  • Demonstrated expertise in the collection and interpretation of X-ray crystallography co-structure data to support NCE optimization
  • Experience with high-throughput crystallography platforms a plus
  • Experience in the preparation and crystallization of membrane proteins a plus
  • Experience with protein biophysical characterizations and screening a plus
  • Strong academic performance demonstrating a track record of high-quality, innovative research
  • Excellent oral and written communication skills, and good presentation skills. Ability to work in a fast-paced, goal-oriented, team environment
151

Senior Scientist Downstream Resume Examples & Samples

  • B.S., in the biological sciences or chemical/biochemical engineering, a related discipline, or its equivalent
  • Graduate education through M.S. or Ph.D. is highly desired.Minimum BS or equivalent with a minimum 13 years BMS/ relevant experience, MS or equivalent with minimum of 10 years BMS/ relevant experience, Ph.D. in Scientific discipline with 4 years of relevant experience in downstream manufacturing technical support or downstream process development in the biopharmaceutical industry
  • Mastery of SOPs, cGMPs and the know how to work and manage within a regulatory environment
  • Proven experience in successful execution and management of process technical transfer
  • Experience in designing and executing process and equipment validation plans
  • Experience in the design, modification and optimization of biologics purification unit operations
  • Proven project management skills that include leading cross functional teams and effectively balancing project assignments with other duties
  • Excellent verbal & written communications skills
  • Interpersonal and facilitation skills necessary to interface with and influence all levels of the organization with the ability to lead people and multi-disciplinary teams
  • 1601517
152

Senior Scientist Resume Examples & Samples

  • Develop and execute laboratory work plans/schedules for self and junior members of team, using customer milestones and Division/site performance standards and metrics
  • Independently authors and approves technical documents, such as protocols, technical reports, batch records, test methods, and operating procedures
  • Review technical documents for accuracy, thoroughness and regulatory compliance
  • Trains, coaches or mentors others on technical, personal development or business issues
  • Responsible as project technical lead on multiple projects, with responsibility for project outcome and customer interaction, including developing customer relationship to grow the business
  • Knowledge of high-shear granulation, fluid-bed technology, roller compaction, compression, encapsulation, and formulation development
  • Uses comprehensive knowledge of principles, concepts and practices and/or techniques to lead complex projects within pharmaceutics department
  • Applies technical and functional knowledge to design experiments/projects that contribute to overall direction of department/ discipline
  • Minimum of 4 years of experience in the pharmaceutical industry is required
  • Hands on experience in oral solid dosage form development and manufacturing is preferred
  • Knowledge of techniques in design of experiments
  • Maintain cGMP and Good Documentation Practices in accordance with applicable regulatory guidance and Site SOPs
  • Advanced project management skills are routinely practiced for multiple concurrent projects of moderate complexity
  • Has substantial breadth/depth of technical acumen in multiple techniques and can understand their application in context of pharmaceutical services offerings
  • Can provide reliable/defendable interpretations of regulatory guidance for the customer
  • Capable of rapid learning of unfamiliar principles or techniques with minimum training
  • Ability to interpret, provide and manage a variety of instructions furnished in written, oral, diagram, or schedule form across multiple work groups
  • Understands the details of regulatory CMC filing package and the drug product documentation required therein
153

Senior Scientist, Large Molecule Resume Examples & Samples

  • A Bachelor's Degree is required
  • A degree earned beyond a Bachelor's Degree (Master's or PhD) is preferred
  • At least four years of related work experience is required
  • Bachelor's degree with >10 years related experience; a Master's degree with >8 years related experience; Doctorate Degree with >4 years related experience
  • Good project management/coordination skills are required
  • Scientific background in GMP analytical and/or business background is preferred
  • Experience with SOP's is required
  • Advanced computer skills ,including significant experience with Microsoft Excel and PowerPoint, are required
154

Senior Scientist Resume Examples & Samples

  • Develop and execute laboratory work plans/schedules independently, using customer milestones and Division/site performance standards and metrics. Sample types include USP, JP, and EP release testing and stability testing. Techniques include but not limited to: sterility, bioburden and microbial limits testing, or endotoxin testing. Responsible for organism identification. Perform and/or guide method validation or transfer activities. Perform and/or guide method development activities
  • Independently authors and approves technical documents, such as protocols, test methods, text reports, certificates of analysis, and operating procedures
  • Understands the details of regulatory CMC filing package and the analytical documentation required therein
155

Senior Scientist Resume Examples & Samples

  • Acts as the technical lead for client development projects (including DOE), communicates project status internally and externally, and effectively provides technical explanation/rationalization
  • Critically analyzes complex data, interprets and integrates experimental results with project objectives
  • Writes complex procedural SOPs, batch production records, and reports
  • Expert knowledge of protein purification and analysis with an in depth understanding of all modes of chromatography
  • Demonstrates expertise knowledge of scale up principles with respect to purification and filtration
  • Demonstrates experience with viral clearance validation and scale down models for biopharmaceutical processes, including review and interpretation of results
  • Leads technology transfer of processes to a cGMP facility
  • Participates in quality control and quality control tracking systems including change control and deviations
  • Manages daily lab operations including oversight of 5S audits, stocking consumables, lab organization and cleanliness, and safety
  • Manages interaction with CRO facilities and vendors that support process development and manufacturing projects
  • Contributes to maintenance of visual control board including tracking metrics, safety updates, and leading daily meetings in absence of director
  • Updates group members on background and status of client projects by giving oral updates or internal presentations
  • Aligns best practices and new technologies with needs of process development and manufacturing departments
  • Troubleshoots and problem solves in order to initiate and execute/monitor corrective actions
  • Performs general lab housekeeping, including cleaning/sterilizing of lab and lab materials, disposal of trash and recyclables, autoclaving, ordering and stocking supplies, etc
  • Performs lab overview for client tours and internal clients (shadowing)
156

Senior Scientist Resume Examples & Samples

  • Provide expertise in process development for numerous mammalian cell lines
  • Initiates, directs and executes scientific development for innovation and process improvements
  • Writes complex procedural SOPs, batch production records, reports and tech transfers to Manufacturing
  • Set-up, operate and troubleshoot single use stirred tank bioreactors up to 250L scale
  • Ph.D. in Biotechnology, or related field with at least 4+ years of laboratory experience in an industrial setting
  • MS in Biotechnology or related field with at least 8+ years of industry laboratory experience
  • B.S/B.A. in Biotechnology, or related field with at least 10+ years of industry laboratory experience
  • Extensive mammalian cell culture experience
  • Operating, maintaining, and troubleshooting stirred vessel bioreactors or fermenters preferably in an industrial setting
  • Strong knowledge of latest upstream process development strategies
  • Knowledge of the optimization of mammalian cell production through media and feed improvements
  • Experience in Tech transfers
157

Senior Scientist, Large Molecule Resume Examples & Samples

  • Hands on experience or knowledge in some or all of the following techniques
  • UV/Vis, Micro Flow Imaging, multi-angle light scattering (MALS), Karl Fischer moisture testing
  • Clear verbal and written communication skills
  • Members of staff within DAS-LMAC
  • Members of staff within other operational Business Units
  • Members of staff within Support Functions
  • Occasional Communication with
  • Members of staff and peers within Other Catalent Business Units
  • Staff within other groups of Catalent
  • Clients and Potential Clients of Catalent
  • Equipment Vendors
  • BS degree in Life Sciences (chemistry, biochemistry or related field) with 7- 10 years relevant experience, or graduate degree with a minimum of 5 years of relevant experience
  • Knowledge/Skills Requirements: HPLC, biochemistry, analytical chemistry
158

Senior Scientist, Large Molecule Resume Examples & Samples

  • Data review
  • Mammalian cell culture
  • Sterile technique
  • Microplate assays (96 well) using microplate readers (some combination of visible, fluorescent and/or luminescent readers)
  • In vitro cell-based bioassays
  • Execution and analysis
  • ELISA assays
  • Understanding of biopharmaceutical regulatory environment
  • To perform checking & verifying of peers analytical data in accordance with in-house SOPs
  • A Bachelor’s degree in biology or closely related science is required
  • Education or Equivalent: BS degree with a minimum of 2 years relevant experience, or graduate degree with no minimum years of relevant experience
  • Large molecule work experience is required
  • Knowledge/Skills/Experience with cGMP, Good Documentation Practices & Data review is required
  • Experience in some or all of the following is required: mammalian cell culture, sterile technique, microplate assays (96 well) using microplate readers (some combination of visible, fluorescent and/or luminescent readers)
  • Experience with at least one of the following is required: in vitro cell-based bioassays, execution and analysis, troubleshooting, ELISA assays, development and/or optimization
  • Understanding of biopharmaceutical regulatory environment is preferred
  • Physical Requirements: Ability to lift up to 44 pounds and stand on feet for extended periods of time
159

Senior Scientist, Biochemistry Resume Examples & Samples

  • PhD in Biochemistry or related field with at least 6 years of post-graduate work experience in epigenetics, as evidenced by an excellent publication record
  • Previous experience in the biopharmaceutical industry with a successful record on project impact and compound progression is highly preferred
  • Strong epigenetic background and understanding of transcriptional regulation
  • Advanced understanding of enzymology and reaction kinetics
  • Characterization of enzyme inhibitors and mechanism-of-action studies
  • Experience in developing robust enzyme assays and miniaturization for high throughput screening
  • Experience with Rapidfire preferred
  • Experience with FRET, SPR, and mass spectroscopy is highly desirable
  • Analysis of both biochemical and cellular structure-activity relationships
  • Ability to write invention disclosures, technical reports, protocols and scientific publications
  • Ability to engage with industry and academic collaborators
160

Senior Scientist, Translational Medicine Resume Examples & Samples

  • Develop strategy, design, execute and interpret experiments to define dose-schedules, patient selection markers and other biomarker readouts, combination strategies and pathways of drug resistance for oncology programs
  • Use cell-based assays and molecular and biochemical profiling to characterize drug mechanism of action, cellular mechanisms of efficacy, and rational drug combinations
  • Lead scientifically on cross-functional and cross-site teams
  • Develop and review study proposals, manage relationships and critically review data from contract labs and academic collaborators
  • Evaluate and advise on clinical trial biomarker/exploratory endpoint strategies, collect and analyze patient data to inform clinical development
  • Subject matter leader
  • Completes technical assignments by designing, executing and interpreting complex experiments
  • Recommends department level strategic decisions
  • Apply diverse scientific knowledge to assignments
  • Interpret results
  • Comprehensive knowledge of tumor cell biology, molecular oncology and cancer immunology; experience developing biologics a plus
  • Working knowledge of a variety of cellular, biochemical and molecular assays, including proliferation/apoptosis, functional assays, flow cytometry, primary cell/3-D and co-culture systems, chemotaxis, ELISA, Western blot, RT-PCR, CRSPR/Cas9 and RNAi
  • Working knowledge of pharmacology models used in cancer biology (including solid tumor and disseminated xenograft, primagraft and syngeneic tumor models)
  • Ability to develop a research plan, conduct experimental work with accurate and detailed record keeping
  • Excellent organizational skills with the ability to efficiently manage and prioritize multiple projects, internal and external collaborations
  • Strong independent problem-solving skills
  • Flexible and adaptable to changing priorities
  • Must be willing to work with a highly motivated team, pursuing goals aggressively
  • The candidate will be a critical experimentalist, results oriented, and enjoy working in a fast-paced environment
  • Excellent teamwork, organizational and communication skills are essential
161

Senior Scientist Resume Examples & Samples

  • Work within a matrix team to develop novel therapeutic approaches for a cell-based immune product in various therapeutic indications
  • Make direct impact on the performance of multiple departments. Impact is achieved by driving team efforts and leading projects
  • Provides input and makes recommendations to research strategies
  • Provides scientific leadership and accountability to accelerate development and to provide insight into cellular product mechanisms and disease biology
  • Independently design and implement long-term project plans, and interpret experiments to define efficacy, combination strategies and mechanism of action of the cellular product via gene, protein and function-based in vitro assessments
  • Improve current functional assessment approaches by designing pertinent novel cell-based assays and/or cellular immune-based assays
  • Participates in management of external collaboration and CROs. Provide recommendations for, and implement studies and strategies to define the potential of the cellular product in pertinent in vivo studies
  • Identify and engage external experts and key opinion leaders to facilitate external assessment or collaborative opportunities to evaluate the cellular product
  • Represents the Research & Development Group in Project team/Franchise team, other cross-functional teams as needed
  • Prepare IND format documentation and / or reports based on scientific results as required
  • Creates disease specific translational goals, and author the translational section of the clinical protocols in trials
  • Creates SOW and interfaces with CRO for execution of services
  • Leads the analysis of translational correlative studies for the clinical studies by working with relevant functions and CRO as needed and generates the study reports
  • Provide scientific leadership to the research team, as well as, create and track achievable goals for the team that are aligned with Corporate and Divisional Objectives
  • The successful candidate should have a PhD or MD/PhD degree in Immune Cell Biology (such as NK Cell, T Cell), Immunology, Translational Science, Oncology, or related field
  • The position requires a minimum of 5 years of hands-on relevant experience with a track record of success as evidenced by a strong publication record, and/or, evidence of sustained contributions in the biopharmaceutical industry
  • Advanced multi-parameter flow cytometry skills are required
  • The candidate must have demonstrated expertise of a wide range of in vitro cellular and biochemical assays, including cell isolation and culture, molecular biology, cellular immunology assays and familiarity with in vivo models of immune disease or oncology are required. Broad knowledge of current scientific areas and technologies
  • Basic understanding of MDS/AML, Lymphoma, Multiple Myeloma, CLL or related hematological malignancies and/or solid tumors
  • Functional area expert with skills, independent critical thinking, theoretical knowledge and experience to apply scientific direction and approach to projects and problems
  • Qualified candidate should be adept at independently designing, executing and interpreting immunology based experimentsThe individual is also expected to establish and manage productive collaborations with academic researchers and contribute to the scientific community by publishing results in high quality journals
  • Proven scientific/leadership expertise, such as working functionally matrixed teams and to mentor junior and mid-level scientific staff
  • Basic understanding of IP, contracting terms and provisions
  • Effective communication is essential and includes presentations to effectively convey scientific concepts and data among research scientists, management teams within internal working groups/project teams, external academic and industrial organizations, review committees, and conferences. Writing for clinical protocols, reports, regulatory filings, and scientific publications is also required
162

Senior Scientist, Genomic Stratification Resume Examples & Samples

  • Pursue and supervise leading computational genomics and patient stratification research towards key Celgene scientific objectives, including coordination and mentorship of junior staff as required
  • Apply contemporary methods for genomic data processing, analysis and mining
  • Collaborate with research colleagues to interrogate clinical phenotypes and develop biomarkers that enable molecular segmentation of key disease subpopulations
  • Guide genomic profiling plans and procurement of high quality genomic data from valuable internal collections of patient biosamples
  • Present and report methods, results and conclusions to a publishable standard, both internally and outside the company where required
  • LI-MG2
  • Ph.D. in bioinformatics, genetics, computational biology, statistics, or related discipline
  • 6+ years post-graduate experience of inter-disciplinary computational and drug discovery research in university, hospital or biotechnology environments
  • Expertise in human genetic and genomic data analysis, interpretation and applied computational research on large multivariate datasets
  • Expertise in the predictive analysis of large datasets, contemporary methods for the processing, analysis and integration of next-generation sequencing data, coupled to extensive domain knowledge in cancer biology and genome science, are prerequisite
  • Experience with integrative analysis and interpretation of diverse datasets, e.g. genomic, transcriptional, functional assay and phenotypic data
  • Deep knowledge of human genomic sequencing methodologies, contemporary processing and analysis pipelines and downstream mining and interpretation approaches
  • Demonstrated experience with biostatistics and analysis of datasets from clinical studies
  • Expertise in algorithmic implementation, statistical programming and data manipulation, using e.g. R/Bioconductor, Matlab, Python, and a range of contemporary, open-source bioinformatics tools and database structures in Linux & cloud computing environments
  • Excellent verbal and written communication skills. Fluent verbal and written English language skills prerequisite
163

Senior Scientist Resume Examples & Samples

  • LI-KA
  • Design and execute formulation, compatibility, and process studies to support phase appropriate development of Dynavax’s drug product portfolio. Duties will include, but not limited to design of programs, evaluation of data, recommendations on strategy, and authoring reports
  • Manage technical transfer efforts and/or manufacturing of new or existing products at CMOs. Support CMOs with the appropriate studies during the development and validation phases of projects
  • Manage and author appropriate development reports and other documents for internal use and support of regulatory filings. Maintain awareness and act as expert on regulatory CMC requirements
  • Supervise research-associate-level staff performing formulation, compatibility, and analytical studies
  • Support the organization in maintaining a work environment focused on quality and that fosters learning, respect, open communication, collaboration, integration, and teamwork
  • This position may travel up to 15%
  • PhD in chemistry, chemical engineering, biochemistry, pharmaceutics, or closely related discipline
  • 10+ years’ relevant industry experience in a pharmaceutical CMC/GMP environment such as process development, formulations, etc
  • Demonstrated expertise in drug product development, including respiratory drug delivery systems
  • Demonstrated knowledge of formulation, process development, CMO management, manufacturing, and regulatory CMC
  • Exceptional written and verbal communication skills to effectively interface across functional teams and present technical concepts and results
  • Must have the ability to identify and resolve critical issues, implement technical, strategic and operational plans
  • Demonstrated team leadership experience
  • Knowledgeable in current pharmaceutical/biological analytical technologies
  • Demonstrated ability to synthesize information to make critical decisions in a timely manner
  • Exceptional interpersonal skills, with proven ability to build positive work relationships across functional lines and to motivate employees
  • Ability to effectively manage multiple projects
  • Personal attributes required include
  • Experience pre-filled syringe presentations a plus
  • Experience with combination products
  • Experience with early phase formulation and process development
164

Senior Scientist Resume Examples & Samples

  • Lead core applied data science activities including data handling, data integration, and data analysis from multi-omics data, including genetics, genomics, transcriptomics, proteomics, and other omics data
  • Develop and implement state of the art data science methods, pipelines, policies, and procedures that contribute to medicines creation platforms. Educate other applied data science team members on these approaches
  • Design and analyze preclinical experiments to guide clinical precision medicine strategies. Analyze clinical data to inform precision medicine strategies for current and future development programs
  • Provide experimental design and analysis as an embedded member of internal cross-functional or global project teams
  • Prepare technical reports including analysis plans, versioned analysis code, statistical methodology, and publications and conference presentations
  • Ph.D. degree in Bioinformatics, Computational Biology, Statistical Genetics, Genetic Epidemiology, Data Science, or closely related field with equivalent experience
  • Must have 3-5 years of relevant experience analyzing multi-omics data. Industry experience is required
  • Must demonstrate expertise in analytics tools for functional genomics and transcriptomics including whole genome sequencing, expression data (including RNAseq), and epigenetics data. Additional statistical genetics experience highly preferred
  • Must have experience applying knowledge-based or data-driven methods for data interpretation (e.g. pathway and network analysis)
  • Must demonstrate advanced analytical and troubleshooting skills and expertise to interpret signals and potential issues with multi-omics data
  • Must have applied experience with advanced statistical methods, i.e., predictive analytics models
  • Must have strong communication skills and the ability to act on cross-disciplinary teams
  • Requires experience with extensive programing skills using R, Python, and Unix/Linux scripting
165

Senior Scientist Resume Examples & Samples

  • Developing high quality biochemical and other in vitro assays ranging in scale from low-throughput to HTS to support drug discovery efforts independently in the wet lab. It includes working with the automation team during assay validation, adaptation and execution on the robot. He/she is expected to deliver results in timely fashion
  • Communicating effectively with internal and external collaborators to achieve company objectives
  • Working effectively in a project team environment
  • PhD with training in biochemistry or structure biology is required
  • 3-5 years industrial experience in related fields
  • A solid track record and experience in assay development
  • Possess solid knowledge in design of fusion proteins and structure biology
166

Senior Scientist, Pathology Resume Examples & Samples

  • Histopathology
  • Manage the GLP Histopathology Test Site operations
  • Principal investigator (pathology)for exploratory, pharmacology and toxicology studies
  • Serve as the Research Project Team Representative
  • Plan and execute nonclinical safety evaluations in support of ongoing projects
  • Design protocols, monitor and review studies conducted at contract research organizations
  • Review clinical protocols and provide information to select appropriate dose
  • Prepare nonclinical safety assessment portion of regulatory submissions and address any inquiries regarding animal toxicity from regulatory agency
  • Evaluate and provide advice to project teams regarding the interpretation of physiological and histopathological data from pharmacology experiments
  • Work with Life Science personnel and biologists to establish in vivo disease models
  • Proactively communicate with project teams (Clinical, regulatory, Biomaker, etc) and collaborate with drug safety units in Japan in performance of the above responsibilities
  • D.V.M or equivalent veterinary degree with ACVP board certification, Ph.D is. desirable
  • At least 3 years of experience in pharmaceutical companies and toxicologic pathology
  • Experience in toxicology, i.e. conduct/summarize toxicology studies, is desirable
  • Highly self-motivated and self directing individual who enjoys working in different environments using multiple capacities and who can seamlessly work across cultures
  • Periodic domestic and international travel required
167

Senior Scientist Resume Examples & Samples

  • Lead the design, execution and interpretation of appropriate purification development experiments to drive the definition and optimization of downstream processes for the generation of recombinant protein active pharmaceutical ingredients
  • Use first principles and designed experiments (DOE) to predict/understand/control the impact of physical and chemical processing conditions on recombinant protein product quality
  • Participate in and/or lead cross-functional process development teams and effectively collaborate with other groups within Lilly and external to Lilly
  • Support transfer of purification processes to internal laboratories, pilot plant and/or other manufacturing sites
  • Lead/support implementation of organizational strategic initiatives in support of Lilly’s pipeline
  • Keep abreast of relevant scientific literature and new technologies/capabilities and regulatory initiatives/requirements. Lead implementation, as appropriate
  • Leverage internal and external influence to solve problems and benchmark potential solutions
  • Support regulatory filings (e.g. information requests, Pre-Approval Inspections, etc.)
  • Provide coaching, training and administration of performance management to personnel (primarily, but not limited to, direct reports)
  • Ensure work and team activities are aligned with all relevant Development, Quality, Regulatory, HSE, GLP and GMP requirements
  • PhD in Chemistry, Biochemistry, or related field with 8+ years of post PhD industry experience
  • Experience in biochemistry with an emphasis on protein chemistry and protein purification
  • Experience in statistics and Design of Experiments (DoE)
  • Exceptional problem solving and decision-making skills
168

Senior Scientist Resume Examples & Samples

  • PhD/equivalent in Cell Biology or Engineering related field with postdoctoral fellowship and 3+ years relevant industrial experience or equivalent
  • Strong background in cell culture techniques and optimization including media formulation
  • Experience with and knowledge of a variety of cell types, including stem cells and primary cells
  • Solid experience and theoretical knowledge of cellular analysis techniques: examples include microscopy, Flow/FACS analysis, immunoassay, PCR, Western blot, ELISA
  • Experience developing new analytical methods
  • Experience with operation of bioreactors and knowledge of downstream processing a plus
  • Ability to give high-energy presentations to external audiences and internal leadership
  • Ability to appropriately communicate with external partners including non-technical partners
  • Excellent organizational skills with ability to prioritize and work effectively on multiple tasks
  • Demonstrated experience in a supervisory role including team building and employee development
169

Senior Scientist Resume Examples & Samples

  • Manage projects and discuss projects with clients when necessary
  • Perform laboratory operations with good dexterity, good laboratory techniques, and high degree of accuracy and precision
  • Document testing, observations, deviations, and results clearly and completely
  • Operate and maintain laboratory equipment, understand principles (theory) of laboratory instrumentation
  • Understand and perform calculations as required by test methods (some derivation of equations may be required)
  • Understand and utilize computers for information access, calculations, processing data, and report preparation
  • Lead projects and perform work utilizing a variety of analytical techniques, act as technical lead in conference calls with clients
  • Train others in laboratory procedures/computer procedures
  • Perform laboratory maintenance, communicate with vendors and repair personnel
  • Write investigations
  • Review developmental and investigational work performed by other analysts when needed
  • Self-teach new analytical procedures and computer programs
  • Write new SOPs and update existing SOPs
  • Experience with ISO 10993 biocompatibility testing
  • Bachelor's degree in Chemistry, Polymer or Materials Science, Biomedical Engineering or related; job experience in the medical device industry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
  • Bachelors with 4+ years’ experience, Masters with 2+ years’ experience or PhD with 1 year experience
170

Senior Scientist Resume Examples & Samples

  • Support a late stage protein drug product process development group in process characterization studies for unit operations including: freeze/thaw, mixing, filling and stoppering
  • Initiate investigations to apply fundamental engineering principles in determining and resolving issues related to the manufacturing of biopharmaceuticals
  • Independently perform bench-scale studies for the physical characterization of drug substances and products
  • Examine individual unit ops and optimize processes, assessing the impact on product quality from different stages of the manufacturing process
  • Identify sources of risk and evaluate the impact of process improvements or changes in equipment, scale, and raw materials on drug product manufacturing
  • Support the technical transfer of the commercial manufacturing process
  • Author process transfer documentation, technical reports, technical assessments, GMP documentation, and regulatory filings
  • Ability to maintain accurate records follow procedures is critical
  • Strong computer, scientific, modeling, and organizational skills
  • Excellent project management skills, multi-tasking, and ability to elevate relevant issues to project lead and line-management
  • Proficiency with Microsoft Office required; familiarity with JMP, Prism, or Minitab a plus
  • Ability to participate in global cross-functional teams and work effectively in a highly matrixed environment
  • B.S. with 4-6 years of experience, M.S. with 2-3 years of experience, with degree in Chemical Engineering, Biochemical Engineering, Pharmaceutical Sciences, or Life Sciences with a pharmaceutical, vaccine, or biotechnology background. Biotech/pharmaceutical industry experience strongly preferred
171

Senior Scientist Resume Examples & Samples

  • Read and understand analytical procedures
  • Perform primary analytical techniques (i.e., electrophoretic [SDS PAGE, IEF], HPLC [reverse phase, size exclusion and ion exchange], and plate reader based assays)
  • Perform laboratory operations with dexterity, and laboratory techniques with a high degree of accuracy and precision
  • Operate and maintain laboratory equipment and understand principles (theory) of laboratory instrumentation
  • Understand and perform calculations as required by test methods (some derivation of equations may be required) then review, approve, and communicate data verbally and in a written format
  • Set up, validate, and perform new analytical procedures or related processes used by the department
  • Prepare documents including (but not limited to) analytical procedures, standard operating procedures, investigations and explanations of analytical results
  • Cross train and provide assistance (if required) in other laboratory areas
  • Lead projects/test areas and perform method transfers and feasibility studies
  • Train others in laboratory and/or computer procedures
  • Communicate with vendors, clients, and repair personnel
  • Perform laboratory maintenance
  • Good understanding of protein biochemistry
  • Understanding of instrumentation theory and analytical techniques as applied to Biopharmaceuticals
172

Senior Scientist Resume Examples & Samples

  • Perform analysis of proteins and the impurities or raw materials associated with their production using various analytical techniques
  • Perform tests accurately
  • Produce written reports (e.g., SOP, OMC, client reports)
  • Initiate and perform investigations
  • Serve as administrator of analytical instrumentation systems
  • Carry out method transfers and feasibility studies
  • Strong protein biochemistry and analytical skills with firsthand knowledge in protein characterization
  • Experience with Mass Spec and HPLC/UPLC
173

Senior Scientist, Hplc Chemist Resume Examples & Samples

  • Perform data analysis and troubleshoot methods and instrumentation
  • Previous experience conducting and analyzing data for analytical methods such as UPLC/HPLC, Dissolution, Thermogravimetric DSC/TGA, and KF titrations
  • Deep understanding of experimentation and data analysis using Empower software (Version III)
  • Excellent technical writing experience in a regulatory environment such as protocols, reports, and SOPs
  • Excellent attention to detail; excellent project management skills including the ability to manage ones project resource requirements (material, manpower, time, etc.), and ability to elevate relevant issues to project lead and line-management
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
  • B.S. and 3-6 years of experience or M.S., 2-4 years of experience in an analytical GMP regulated environment
174

Senior Scientist Resume Examples & Samples

  • Literature search & toxicity/safety data collection for identified issues seeking toxicology support
  • Literature review for hazard assessment of ingredients intended to be used in consumer and OTC products and preparation of their toxicology profiles
  • Assessment and approval of fragrances and flavors used in consumer and OTC products
  • Risk assessment for raw materials and formulations for cosmetic applications including Margin of Safety calculations
  • Safety assessments for impurities and degradents as per regulatory requirements
  • Review of formulae at different stages of product development cycle
  • Preparation of California proposition 65 reports
  • Addressing and evaluating the risk of compliance issues raised by regulatory authorities & QA, and impurity qualification
  • Master’s degree in toxicology, pharmacology or relevant science discipline
  • 3-5 years of experience in the field of consumer product risk assessment or other relevant Toxicology experienceToxicology Research
175

Senior Scientist Bioanalytical Services Resume Examples & Samples

  • Aid in the development of bioanalytical methods
  • Validate unique scientific methods, assays, techniques, reports, etc
  • Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment
  • Communicate project timelines, status, and data to Principle Investigator effectively addressing any issues that may arise
  • Simultaneously handle method development & routine sample analysis projects as required
  • Coordinate study activities with Principle Investigator to ensure efficiency and quality
  • Ability to work on multiple projects at the same time
  • Coordinate with Project Management and QC for timely sample analysis and results assessment
  • Aid in the preparation of study summaries and/or reports
  • Research literature and external sources and identify new techniques and procedures that strengthen Frontage’s capabilities
  • Help with training and/or mentoring of junior scientific staff
  • Set-up, utilize, and maintain complex instrumentation
176

Senior Scientist / Scientist Resume Examples & Samples

  • Develop new NGS library preparation assays and kits in fast-paced product development environment. In collaboration with multi-disciplinary teams, design, develop and launch state-of-the art products compatible with Illumina sequencing and library preparation platforms
  • Design, implement, analyze and present experiments to demonstrate feasibility of new methods and efficiently move products through pipeline
  • Write reports and present results and project assessments to Senior Management
  • Perform equally well as individual contributor, collaborative team member and technical manager depending on project needs
  • Lead projects and guide technical areas independently
  • Make decisions involving designing, performing, troubleshooting, analyzing and presenting experiments
  • PhD in the Biological Sciences (biology, biochemistry, chemistry) or closely related discipline
  • 4+ years’ post-PhD industrial experience in biotechnology
  • Strong background in biochemistry and molecular biology with a sound understanding of genetic assay development
  • Experience designing and developing Targeted Sequencing, Amplicon & Enrichment Library Preparation Systems
  • Experience with Next Generation Sequencing required and experience with Illumina platforms is preferred
  • 3+ years’ experience in commercial product development with demonstrated record of product launch and transfer to operations
  • Proven record of transferring new products to manufacturing and/or QC in a fast paced biotech environment
  • Able to work effectively under pressure to meet scheduled deadlines and handle multiple activities simultaneously
  • Excellent oral and written communication skills required to clearly explain complex issues, progress reports and technical roadmaps
  • Ability to translate corporate and project goals into executable experimental plans understanding technical risks, mitigations and alternatives
  • Demonstrated ability to efficiently analyze Sequencing data
  • Highly motivated, meticulous individual with the proven ability to think innovatively toward solving problems effectively and efficiently
177

Senior Scientist, Protein Engineering Resume Examples & Samples

  • Build libraries for protein engineering program at IPD and other divisions
  • Work in partnership with project teams to support their specific needs
  • Support screening and analysis of protein libraries in a variety of microbial hosts
  • Develop and improve molecular tools for library construction, and work with external providers where appropriate
  • Maintain timely and accurate documentation of laboratory work
  • Ph.D. in molecular biology, biochemistry, or related field
  • 5+ years of experience in an industrial setting
  • Demonstrated proficiency with a variety of library construction methods
  • Familiarity with operation of automated liquid handlers and other laboratory instrumentation
  • Solid grasp of statistical analysis of large data sets
  • A strong desire to grow as a scientific researcher, learn new techniques and adopt new technologies
  • Ability to reach rational conclusions through processing of complex information
  • Flexible to change and strives for continual improvement of themselves and the team
  • Well organized and capable of clear communication in both oral and written forms
  • Ability to think and adapt to a rapidly changing environment
  • Able to reach rational conclusions through complex processing of information
  • Proficiency with MS Office suite
178

Senior Scientist Resume Examples & Samples

  • A minimum 5 years of experience in biology, microbiology, virology, immunology, or related field
  • Strong scientific skills including protein expression, purification and characterization along with molecular biology experience are preferred
  • Experience in working with animal health industry
  • Knowledge of regulatory requirements for vaccine registration
  • Proven problem solving and listening skills along with sound judgment and business integrity
179

Senior Scientist Resume Examples & Samples

  • Experience in peptide or macrocycle synthesis, purification and analytical characterization including HPLC, MS and biophysical methods
  • A strong track record of peer-reviewed publications and research presentations
  • Ability to mine scientific literature and databases
  • Ability to train team members in aspects of peptide synthesis
  • Experience in communication and collaboration skills in a team environment
180

Senior Scientist Antibody Expression Resume Examples & Samples

  • Hands on experience in mammalian cell culture within a BSL-2 environment
  • Experience in antibody generation in transient transfections of HEK and CHO cells at various scales
  • Experience in developing stable cell pools and clones for both secreted and membrane-bound proteins
  • Experience with automated liquid handling system is preferred
  • Hands-on experience and technical expertise in molecular biology techniques, including PCR, cloning, DNA and RNA purification, SDS-PAGE and Western Blot
  • Familiarity with key bioinformatics tools
  • Experience in leading cross functional biologics discovery projects preferred
  • Experience in the pharmaceutical or biotechnology industry is expected
181

Senior Scientist Resume Examples & Samples

  • Experience working in biopharma with monoclonal antibodies
  • Demonstrated ability and expertise in analytical method execution, optimization, characterization and data analysis, with technical experience in some of the following analytical methods
  • Knowledge and experience with chromatography software, such as Empower 3
  • Proficient in MS Word, Excel, PowerPoint, etc
  • Working understanding of US/EU regulatory requirements and / or working knowledge of cGMPs is a plus
182

Senior Scientist, Computational Chemistry Resume Examples & Samples

  • No more than 5 years of drug discovery experience in industry
  • The ability to work well in multidisciplinary teams
  • Evidence of creative application of computational approaches to problems of pharmaceutical interest
183

Senior Scientist, Hybridoma Resume Examples & Samples

  • Design and implement immunization strategies to multiple target classes
  • Isolate immune cells from spleen and/or lymph nodes and perform fusions
  • Perform screening assays for binding and function and present results at project team meetings
  • Expertise in cell culture
  • Strong written and verbal communication skills in a team-oriented environment
184

Senior Scientist, Process Chemistry Resume Examples & Samples

  • Experience in methodology/catalysis (including chemocatalysis, biocatalysis and heterogeneous catalysis), total synthesis, physical organic chemistry, or flow chemistry
  • A proven track record of solving complex problems
  • Candidates must possess strong written and oral communication skills, and the ability to work effectively in a team environment
  • Function well within multidisciplinary teams and possess outstanding communication skills
  • Strong problem solving and troubleshooting skills
  • Strong leadership and interpersonal skills
185

Senior Scientist Resume Examples & Samples

  • A Doctorate OR a minimum 4 years with MS OR 6 with BS of experience in a similar role in pharmaceutical drug development or academia, with a record of increasing responsibility and independence
  • Strong skills in experimental design, mathematical problem solving, critical data analysis/interpretation, statistics, and hands-on computer modeling (including proficiency with one or more of the following software packages, such as, but not limited to: NONMEM, Matlab, sPlus, R, WinNonlin)
  • Solid proficiencies in written and verbal communication, interpersonal skills, problem scoping and planning, and the ability to participate in and lead interdisciplinary teams
186

Senior Scientist Resume Examples & Samples

  • Leading a small process development team to execute lab-scale process development, in-process assay support, and process scale-up of cell culture/fermentation (upstream) and/or purification processes (downstream) unit operations
  • Partnering with commercial manufacturing teams to support facility start-up activities and provide on-the-floor support for drug substance manufacturing, both within the Merck network and at contract manufacturing organizations (CMOs)
  • Authoring and/or reviewing technical documents to support Process Performance Qualification (PPQ) and licensure
  • Leading technical support activities for licensed vaccines, as needed
  • Five (5) years of large molecule drug substance experience
  • Three (3) years of experience with process development experience in a laboratory setting or three (3) years of experience within pilot-scale, or manufacturing environment
  • Subject Matter Expertise with lab or pilot-scale fermentors/bioreactors and/or large molecule purification (chromatography, filtration , centrifugation)
  • Experience authoring technical documentation to support regulatory submissions
  • One (1) year experience mentoring junior colleagues
  • Strong problem solving and communication skills
  • Experience with on-the-floor support including providing immediate responses on the shop floor to deviations and potential deviations
187

Senior Scientist Resume Examples & Samples

  • Knowledge of neuroscience and neurological diseases
  • Knowledge of genetics
  • Previous work with large-scale datasets, statistical skills and the ability to query databases
188

Senior Scientist Engineering Resume Examples & Samples

  • Provide technical support and leadership for drug substance development and characterization teams including the design, execution, and interpretation of lab-scale, pilot scale and manufacturing scale elements of technical program to ensure processes are suitable for PPQ, licensure, and commercial manufacturing
  • Support definition and development of process control strategy
  • Support continuous improvement of post-launch manufacturing process
  • Identify and evaluate new/innovative technologies and work to implement new platforms with cross-functional early and late stage development teams
  • Manage technical programs including establishing and delivering on project timelines and milestones
  • Partnering with commercial manufacturing teams to provide upstream subject matter expertise to support ongoing manufacturing activities
  • Commercialization experience in biologics, vaccine or other therapeutic proteins
  • Deep technical knowledge and in-depth experience with upstream process development
  • Experience with Quality by Design (QbD), Design of Experiments (DOE), and Lean Six Sigma principles
  • Solid experience in using software and statistical tools for data mining, data analysis and modeling is key
  • Advanced computer skills using MS Office Suite (Outlook, Word, Excel, Power Point etc.),
  • Knowledgeable in Drug Substance, end to end process development
  • Strong cross functional background, enabling teams to reach peak performance
  • Ability to provide scientific mentorship and guidance to technical coworkers and colleagues within and outside of Merck
  • Experience supporting/writing regulatory filings (IND, BLA) and inspections with multiple agencies (FDA, EMA, JNDA,)
189

Senior Scientist, Engineering Resume Examples & Samples

  • Manages and is responsible for the quality level of downstream related process development studies and documentation
  • PhD with no years experience
  • Masters with two years applicable experience
190

Senior Scientist, Global Vaccines & Biologics Resume Examples & Samples

  • Technical expertise in purification of biological molecules to include laboratory skills in chromatography and filtration systems. 
  • Experience with downstream purification of biological molecules required, with an in-depth knowledge of preparative chromatography, tangential flow filtration, and virus retaining filtration desired.  Demonstrated understanding of the fundamentals and/or modeling of unit operations is a plus
  • Technical operations experience in the manufacture of biological molecules at the pilot- and/or commercial-scale is a plus. 
  • Proven experience with execution of laboratory studies to support late stage bulk process development including viral clearance studies, process characterization and process validation studies
  • Experiences in site readiness, batch record reviews, authoring regulatory BLA sections and/or working with external contract organization for development and or manufacturing is a plus
  • Working knowledge of statistical methods for DOE design and data analysis (e.g., JMP or Design Expert software's)
  • Working understanding of analytical methods to characterize biologics and /or US/EU regulatory requirements and / or working knowledge of cGMPs is a plus
191

Senior Scientist, NMR Spectroscopist Resume Examples & Samples

  • A minimum of 1 year of experience in the use of NMR methodologies in the area of small organic molecule structure elucidation (e.g., natural products, pharmaceuticals, etc.)
  • Experience in the implementation, set-up and fine-tuning of new NMR experiments
  • Proficient with NMR pulse programming (Bruker)
  • Experience in structure elucidation of organic compounds, small molecules and natural products
  • Experience in the use of Bruker and Agilent NMR software and hardware
  • Technically inclined with the ability to troubleshoot instrument problems
  • IT literate with the ability to manipulate data work-flows in a networked environment (e.g., Linux and Windows OS, macros, scripts, etc.)
  • Good working knowledge of organic chemistry
  • Customer focused and driven to continually work towards technical and process improvements
  • Excellent interpersonal and leadership skills
192

Senior Scientist Resume Examples & Samples

  • Development of medium to high throughput cell-phenotypic and biochemical assays for proof-of-concept functional studies, target validation and compound screening
  • Validation of hit compounds for follow-up mechanistic studies and lead-optimization
  • Maintaining broad knowledge of literature and state-of-the-art technology
  • Communicate results at team and departmental meetings
  • Interface broadly with GpGx scientists, Discovery, and Preclinical Pharmacology teams
  • Deep understanding of and hands-on experience working on development and implementation of cellular and/or biochemical assays for support of genetic or compound screening
  • Experience in working with human and murine in vitro and ex vivo cellular models (mammalian immortalized and primary cells)
  • Direct experience in development of immunoassay on multiple platforms such as MesoScale, Luminex, Opera etc
  • Experience in, or aptitude for, technologies including CRISPR genome editing and/or RNA interference
  • Knowledge in the development of reporter cell lines (i.e. GFP, Luciferase)
  • Strong communication, collaboration, and including an ability to communicate experimental design, results and conclusions in a clear and concise manner to biologists, chemists, and senior management
  • Other requirements include strong data analysis skills, and high level of flexibility to thrive in a fast paced and dynamic environment
193

Senior Scientist Resume Examples & Samples

  • Independent leadership of projects with minimal supervision
  • Witten and verbal communication of study plans and results to project lead and more broadly at team and departmental levels
  • Experience in establishing and working with human and murine in vitro and ex vivo cellular models (iPSC, mammalian immortalized and primary cells)
  • Direct experience in development of immunoassay or high content imaging assays on multiple platforms such as MesoScale, Luminex, Opera etc
  • Experience in, or aptitude for, technologies including CRISPR genome editing, RNAi and reporter cell line generation
  • Understanding of disease area biology including cardiometabolic, immunology, or neuroscience
  • Strong communication, collaboration, and leadership skills, including an ability to communicate experimental design, results and conclusions in a clear and concise manner to biologists, chemists, and senior management
  • Other requirements include strong data analysis skills, and high level of flexibility to thrive in a dynamic environment
194

Senior Scientist Resume Examples & Samples

  • Development of medium throughput cell-phenotypic assays for proof-of-concept functional studies, target validation and compound screening
  • Validation of hit genes and compounds for follow-up mechanistic studies and lead-optimization
  • Interface broadly with GpGx and Neuroscience Therapeutic Area scientists, Discovery, and Preclinical Pharmacology teams
  • Expertise in neuroscience
  • Expert knowledge in establishing and working with human and murine in vitro and neuronal models, such as human iPSC derived neurons OR primary rodent neurons cells
  • Direct experience in development of in vitro phenotypic assays such as high content imaging, FLIPR and multi-electrode array (MEA)
  • Experience in, or aptitude for, genomics technologies such as CRISPR, RNAi and in vitro viral delivery methods
195

Senior Scientist Resume Examples & Samples

  • Design, optimize, and characterize purification processes for the manufacture of monoclonal antibodies, bispecific antibodies and antibody fragments in early stage (Phase 1/Phase 2) clinical development
  • Act as a subject matter expert in support in troubleshooting and resolving deviations in GMP manufacturing processes
  • Make periodic presentations in group meetings, project team meetings, and in one-on-one situations
  • Prepare technical reports
  • Execute Scale-up studies
  • Support technology transfer to the Clinical Manufacturing facilities
  • Experience performing basic analytical techniques for protein products (HPLC analysis, protein quantification methods, electrophoresis; etc.)
  • Working knowledge of AKTA systems/software
  • CGMP manufacturing experience
  • Knowledge of process robustness concepts and process scale-up
  • Passion for fighting cancer
196

Senior Scientist, Topicals & Transdermals Resume Examples & Samples

  • Designing, planning and overseeing the conduction of pharmacology, safety pharmacology, and toxicology studies designed to address specific regulatory issues
  • Author and review research reports, protocols, guidelines and SOPs for the department
  • Provide support in the research and construction of regulatory study documents, technical scientific analyses and positional papers (i.e., IND/NDA documents, Applications for Marketing Authorizations, etc.)
  • Must possess knowledge of the biological impact of drug materials in the human body and application of GLP and ISO regulations is required. Knowledge of applicable world health authorities’ regulations, standards and guidelines covering topical and transdermal drug development is essential
  • Must possess effective organizational, oral and written communication and computer skills. Must be able to interact with a diverse workgroup in a team-oriented environment with the ability to communicate performance expectations in a clear and concise manner
  • Position functions semi-autonomously. Position directly supervises employees. Carry out supervisory responsibilities in accordance with the organization's policies and applicable laws. Responsibilities may include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems
  • Ability to solve equations, apply technical mathematical concepts, and perform complex computations
197

Senior Scientist, Generics Resume Examples & Samples

  • Assess and resolve impurity, degradant and device-related qualification issues
  • Designing, planning and overseeing the conduction of pharmacology, safety pharmacology and toxicology studies
  • Comprehension of relevant Mylan Standard Operating Procedures (SOPs) and compliance with Laboratory SOPs and other relevant policies
  • Represent the department and Mylan in meetings with global regulatory health authorities and attending internal meetings
  • Must possess knowledge of the biological impact of drug materials in the human body and application of GLP and ISO regulations is required. Knowledge of applicable world health authorities’ regulations, standards and guidelines covering drug development is essential
  • Ability to solve problems with complex variables through non-standardized solutions that require independent judgment and analysis. Ability to draw inferences and use deductive reasoning with no prescribed procedures to solve complex problems
198

Senior Scientist, Bioanalytical Resume Examples & Samples

  • Devise bioanalytical method development strategies for the quantitation of therapeutic protein drugs, anti-drug antibodies, and neutralizing antibodies
  • Work with Contract Resource Organizations (CROs) to transfer assay methods. Review method validation data and Review analytical study data reports generated by third parties and/or CROs
  • Write/review method validation and analytical study plans. Write test method procedures as required
  • Perform method development laboratory work as required
  • The preferred candidate will have a Ph.D. and at least 2 years of relevant experience. However, a combination of experience and/or education will be taken into consideration
  • Must possess experience developing ligand binding based assays for the determination of protein therapeutics and/or anti-drug antibodies (ADAs) in biological fluids
  • Experience with multiple relevant assay formats (e.g. ELISA, MSD, cell-based assays) is preferred
  • Experience working in a regulated environment and familiarity with Good Laboratory Practice (GLP) regulations is preferred
199

Senior Scientist Resume Examples & Samples

  • Designs experimental and data-analysis studies to further develop the TruCulture platform. This will include optimizing protocols, designing new features, developing new applications, contributing to regulatory filings, and working with collaborators to develop clinical diagnostic tests
  • Performs experiments, makes detailed observations, analyzes data, interprets results, organizes and write-ups experimental protocols, data summaries, experimental and technical reports
  • Participates in development of intellectual property, marketing, and technical support materials such as various presentation slides, product feature-based competition analysis reports or preparation of technical documents for regulatory submissions
  • Demonstrates accuracy and thoroughness. Looks for ways to improve and promote quality. Monitors his or her own work to ensure quality. Embraces and applies feedback to improve performance
  • Demonstrated excellence in the development, implementation, and processing of in vitro assays, including cellular and flow cytometric assays
  • Data analysis skills, including familiarity with multi-plex biomarker data analysis as well as standard statistical analysis practices
  • Strong cell culture skills including whole blood cultures and PBMCs
  • Self-motivation and the ability to work independently, and collaborate as part of internal and external cross-functional teams
200

Senior Scientist, Technical Services Resume Examples & Samples

  • Collect, review and analyze formulation and process data to facilitate formulation and process control and improvement
  • Work with R&D, Manufacturing, and Quality departments to identify Critical Process Parameters, Critical Material Attributes, and Process Control Strategies
  • Analyze annual product review data and assist in defining corrective actions for problematic products
  • Assist in educating and training tech services colleagues and manufacturing personnel in critical technical formulation and processing aspects of assigned products
  • Keep current with all Federal guidelines, technical innovations, and topics of current interest regarding formulation, process control and improvement and validation
  • Minimum of a Bachelor's degree (or equivalent) and 2-4 four years of experience. However, a combination of experience and/or education will be taken into consideration. A Bachelor's degree in a scientific field is required. Desired candidates should possess a M.S. or Ph.D. degree in a scientific field such as Pharmaceutics, Engineering, or Chemistry and have at least five years pharmaceutical industry experience with emphasis on drug development, process development, or manufacturing
  • Demonstrate comprehensive understanding of solid oral dosage form manufacturing, process optimization, scale-up, and investigations. Must be proficient in statistical based experimental design and interpretation of results. Must have working knowledge of cGMPs, Standard Operating Procedures, FDA regulations and safety
  • Must possess strong writing, communication, comprehension, interpretation, problem solving, team, critical thinking, and organization skills. Must possess the ability to use creativity to solve formulation and process problems and make sound decisions in manufacturing situations. Must possess excellent technical computer skills
201

Senior Scientist, Organic Synthesis Resume Examples & Samples

  • Route selection for the most efficient way to synthesize the required compounds
  • Extensive lab work designing and executing experiments, and analyzing resultant data
  • Process optimization and scale-up
  • Establishing the right set of the documentation, related to products production
  • Collecting and analyzing the analytical data
202

Senior Scientist / Scientist Resume Examples & Samples

  • Ph.D. in Molecular Biology, Chemistry Engineering or other relevant disciplines
  • Proven hands-on experience with bioreactor, wave-bag or other scale-up cell culture technologies is a must
  • Expert knowledge of cell culture scale-up for mammalian cells, yeast and bacteria
  • Familiar with batch and fed-batch culture technologies for recombinant protein production
  • Experience from a biotech/pharmaceutical R&D setting is desired
  • Good communication skill and team spirit
  • Innovative, flexible, open to new ideas
203

Principal / Senior Scientist Resume Examples & Samples

  • Develop and implement engineered cell lines in bioassays
  • Define scientific approaches and analysis methods for quantitative bioassays
  • Participate in the development, qualification and transfer of bioassays
  • Take leadership role contributing to the scientific literature
  • Ensure timely completion and delivery of analytical results and documentation (technical reports, SOPs, etc.) to support product development during clinical phases
  • The role will have line management responsibilities of research associates and/or scientists, which requires a strong commitment to mentoring staff and promoting their individual growth and development
  • PhD in Biological Sciences (Cell Biology, Biochemistry, Immunology or related field) with a minimum of 6 years (Principal Scientist) or 2 years (Senior Scientist) of relevant industry experience
  • Experience in developing and analyzing quantitative cell-based and biochemical/immunological assays in the context of relative potency
  • Understanding of MOA for gene therapy and/or antibody-based therapeutics
  • Familiarity with software packages to analyze dose-responses and statistical analysis (SoftMax, JMP, etc)
  • Highly motivated and comfortable working independently in a fast-paced environment
  • Demonstrated ability to work in a matrixed environment and interact productively with scientists at various levels, both locally and internationally
  • Experience in a GMP compliant environment
204

Senior Scientist Resume Examples & Samples

  • Requires a Ph.D. degree in the life sciences with 3-5 years of relevant lab experience in academia or industry
  • Experience and knowledge of cutting-edge cell culture and molecular techniques
  • Demonstrated success with mammalian cell expression systems and stable cell line or cell pool generation experience are essential
  • A strong background in the molecular aspects and biology of antibodies is a decided asset
  • Expertise using the WAVE bioreactor platform or other bioreactor platforms is highly desired
  • A track record of developing and/or accessing and employing new technologies relevant to the field of protein expression
  • The candidate should have excellent communication skills, and the ability to manage multiple projects working transversally and in a collaborative team environment
205

Senior Scientist, Downstream Process Resume Examples & Samples

  • Drive 2nd/3rd generation LCM process development & support key strategic initiatives (such as Facility of Future)
  • Lead Tech transfer, scale-up development & adaptation, process control strategy, process validation, comparability for TMabs products introduction at Sanofi and external Industrial sites
  • Provide technical assistance to commercial manufacturing and QC at sanofi & external sites including change assessment, process monitoring, troubleshooting and continuous improvement
  • Contributes to setting up, managing, and evolving a lab unit with focus on downstream purification process (DSP) such as chromatography and filtration
  • Lead the design and execution of experiments in protein chromatography, viral inactivation, ultrafiltration/diafiltration operations. Author technical documents including protocols, reports and SOPs supporting
  • Support process development and improvement, process control strategy, commercial manufacturing operations, global technology transfer, process validation, and regulatory filings
  • Lead or contribute to troubleshooting process related problems observed at manufacturing scale and evaluation of new process technologies through the effective design of scale-down studies and the evaluation of data from manufacturing lots
  • Provides technical expertise for global MSAT process and analytical topics, LCM projects, commercial operation. Represent MSAT in cross functional teams for initiatives, innovations and alignment
  • Work collaboratively with upstream, downstream and other support service functional groups to ensure timely completion and smooth communication of established milestones
  • Provides technical support and guidance for the design, development, scale-up, optimization, monitoring, and/or operation of robust, cost effective, and scalable processes
  • Keep current on contemporary industrial standards, practices and technology focused on the full range of downstream process and ways of performing lab studies
  • Maintain awareness of current process and product control strategies, and contributes to improvement in process understanding and in-process control strategies
  • Contributed to build/adapt & deployment of best practices and technical way of working within TMabs development and manufacturing teams. Contribute to internal documentation and preparation of reports required for regulatory documents
  • Provides scientific mentorship to junior staff. May supervise a small lab operation team
  • Represents global MSAT in the greater biotech community by publishing in peer review journals and participation in scientific/technical conferences
  • Degree in chemical /biochemical engineering, or biological and biochemistry sciences, or related disciplines ; BS with 10+ years OR, MS with 8+ years OR PhD with 5+ years relevant experience
  • Hands-on experience in biologics development, bioprocess engineering and/or commercial manufacturing operations
  • Hands-on Laboratory/pilot or manufacturing skills in downstream process such as centrifugation, depth filtration, chromatography, viral filtration, tangential flow filtration. Knowledge of protein analytical and characterization techniques such as HPLC, iCIEF, CE-SDS, Elisa, and qPCR is a plus
  • Prior experience with leading projects and mentoring technical staff preferred
  • Prior experience with process deviation investigation and implementation of process improvement in manufacturing scale is a plus
  • A strong understanding of the fundamentals of chromatography and /or membrane separation preferred
  • Solid scientific background, strong verbal, written and presentation communication skills is integral to this position
  • Act for Change – Creatively challenges the status quo to find new ways of working
206

Senior Scientist, Gene Thereapy Resume Examples & Samples

  • Ph.D. in Molecular Biology or related discipline and 3-5 years related experience
  • Working experience with AAV platform technology
  • Publication record in Gene Therapy, especially in the ocular or CNS areas
  • Experience in AAV production and purification is a plus
207

Senior Scientist, Gene Therapy Resume Examples & Samples

  • Ph.D. in Molecular Biology or related discipline and 3-5 years of experience
  • Working experience with AAV platform technology or gene therapy therapeutic applications
  • Ability to work in a collaborative environment
  • Publication record in gene therapy, especially in liver diseases
208

Senior Scientist, Gene Therapy Development Resume Examples & Samples

  • Manage the Gene Therapy downstream process development staff
  • Lead the design of and execution of experiments supporting the generation of a purification strategy for the production of viral gene therapy vectors. The individual will apply principles and theories in area of responsibility to develop state-of-the art processes and advance programs. Evaluate new technologies and develop strategies for their implementation in Gene Therapy process development
  • Lead process scale-up activities, including execution of manufacturing scale runs; may act as a subject matter expert supporting the transfer of process technology to both internal and external clinical manufacturing groups
  • Author protocols, technical reports, data analysis summaries, and SOP's
  • Use scientific principles and experiential knowledge to solve complex problems in creative and practical ways
  • Ph.D. in Chemical Engineering, Biochemical Engineering, Bio (medical) engineering, Cell Biology, Biochemistry or related fields with a minimum of 3-5 years of relevant industry experience
  • Must have demonstrated skills and working knowledge of the unit operations associated with biologics manufacturing - column chromatography (operation of manual and automated chromatography systems), TFF, depth filtration
  • Fundamental understanding of typical molecular analytical methods (e.g. qPCR, SDS-PAGE, etc.)
  • Understanding of regulatory requirements for Phase I/II CMC; experience in application of QbD to process development and process characterization
209

Senior Scientist, Dmpk Translational Research Resume Examples & Samples

  • Design, execute, and report key biomarker data to support compound progression and translational research strategy for programs from target loading through early clinical development
  • Work with project teams to address biomarker strategy through candidate selection
  • Collaborate with biology, pharmacology, and modeling and simulation colleagues to design and conduct PK/PD and/or efficacy studies to support translation and clinical dose setting
  • Evaluate and develop biomarker assays via LC-MS/MS technologies, ligand-binding assays, or other appropriate assay systems
  • Contribute equally with other project team members on high level project strategy
  • Work closely with department colleagues to coordinate work for project teams
  • Keep an accurate notebook according to company policy
  • Communicate with colleagues effectively
  • Follow company safety procedures
  • PhD with post doc in Pharmacology/Biochemistry/Life Science or related coursework with 4+ years of relevant industry experience OR MS/MA with 14+ years OR BS/BA 16+ years industry experience
  • Experience in developing fit-for purpose biomarker assays for the measurement of proteins, peptides, and antibodies
  • Expertise in development of quantitative analytical bioassays from complex matrices is required
  • Thorough understanding of application of biomarkers to understanding exposure-effect relationships
  • Knowledge of drug discovery process, DMPK function and pharmacology is required
  • Demonstrated ability to work within a matrix and team environment
210

Senior Scientist, ADL Resume Examples & Samples

  • Contributes significantly to complex/multiple projects or functional areas through leading or influencing others
  • Influences and supports initiatives related to driving scientific and technical improvement within function and potentially cross-functionally
  • Coordinates with others in creating technical reports including reviewing and editing
  • Identifies process trends and defines/champions process strategy or use of novel technologies
  • Represents functional area on GCT project teams by communicating activities from designated functional area to project team
  • Ensures a productive and development-rich environment; provides training/mentoring for junior staff
  • Qualified candidates should possess a Masters degree with 9+ years (all in analytical chemistry or a closely related field) and work experience in a pharmaceutical analytical development laboratory with a working knowledge of cGMPs; (or)
  • Qualified candidates should possess PhD with 3+ years (all in analytical chemistry or a closely related field) and work experience in a pharmaceutical analytical development laboratory with a working knowledge of cGMPs
  • Previous experience as an analytical lead on CMC project teams is desired
  • Technical capabilities include, but not limited to, advanced knowledge/experience of HPLC, GC, dissolution apparatus, KF, UV-Vis and FT-IR. Experience in use of LC/MS, GC/MS, SFC, NMR, DSC, TGA and particle size analyzer will be a plus
  • Experience in the analytical development of linker molecules used in ADCs (antibody drug conjugates)) is desirable
  • Non-technical capabilities include, but not limited to, project management skills, effective interface with drug substance and drug product development groups, strong written and oral communication skills, resource management skills and an influential team player in a cross-functional environment
  • Communication Skills -Able to expresses one’s self clearly and concisely within team; documents issues and/or concerns concisely with colleagues; adjusts communication style as appropriate for the audience; timely and effectively communicates with senior management; technical writing skills to support authorship and approval of internal technical documents
  • External Involvement – Demonstrated involvement in professional community evidenced by presentation of scientific posters or lectures at professional conferences or events. Interacts with external vendors for projects
  • Strong knowledge of analytical techniques with advanced experience in multiple techniques such as LC, GC, MS, dissolution, etc; Able to work in lab setting; Experience representing AD in a cross functional CMC environment; Multiple experiences with methods development, validation and transfer; Ability to design and direct analytical strategy to meet CMC project objectives
211

Senior Scientist Resume Examples & Samples

  • Lead and manage efforts between different teams, e.g. Vaccine Technology and Engineering, Process Development, Bio-analytical, Discovery and Preclinical, including scheduling and compilation of data as it becomes available
  • Support the Head of Formulation development in project development strategies and planning and execution of deliverables
  • Design and execute or oversee studies performed in-house or by contract testing organizations (CTOs)
  • Design and execute or oversee studies performed in-house to improve product performance and maximize shelf
  • Develop methods to improve existing techniques and/or methods sourced from journal articles and/or other scientists
  • Provide expertise to support third parties, R&D and other functions as required to achieve the project goals and priorities
  • May participate in scientific conferences and/or author manuscripts for submission to scientific journals
  • Good oral communication and demonstrable, exemplary writing skills
  • Well-developed knowledge of cGMP practices as applicable to formulation, analytical development, technology transfer, or manufacturing
  • Well organized and detail oriented, with ability to effectively prioritize tasks, eager to learn, interact cooperatively and effectively with others in a team environment, and consistently demonstrate reliability and responsibility
212

Senior Scientist, Vaccine Discovery Resume Examples & Samples

  • Lead discovery activities for one or more project to develop candidate live-attenuated, inactivated, or recombinant vaccines through pre-clinical evaluation
  • Effectively manage a scientific team, including promoting a culture of team accomplishment and providing career development
  • Design program and lead team to execute complex vaccine development activities in support of regulatory filings for new vaccine candidates or those already in clinical development, including
  • Lab-scale processes for seed virus generation and antigen production
  • Analytical method development to quantitate potency and characterize vaccine components
  • Immunogenicity and efficacy models and immune assays to quantify immune responses in pre-clinical studies
  • Novel immunogenicity and virology assays for exploratory clinical endpoints
  • Analyze, interpret and summarize complex data and contribute to project decisions
  • Propose, establish and lead collaborative projects with academic and corporate collaborators or CROs
  • In collaboration with clinical development, design and execute R&D studies to characterize human clinical immune responses to candidate vaccines in development
  • Collaborate with process development and CMC in the transfer of analytical methods and vaccine candidates
  • Present project plans, status and results in internal and external meetings and publications
  • Ph.D. in a scientific discipline with a minimum of 12 years vaccine development experience , MS in a scientific discipline with a minimum of 14 years vaccine development experience, or a BS in a scientific discipline with a minimum of 16 years vaccine development experience
  • Proven ability to design and develop viral vaccines, including scientific accomplishment in virology, molecular biology, immunology or related field
  • Scientific management experience, including demonstrated experience managing laboratory personnel in a team environment and a working knowledge of scientific project management
  • Significant industry experience and working knowledge of GLP practices
  • Exemplary oral and written communication skills
  • Compliance with Takeda safety practices and standard operating procedures
213

Research / Senior Scientist, Biomarker Resume Examples & Samples

  • Experience in the pharma or CRO industry supporting bioanalysis of large molecules and the development of biomarkers to support drug discovery and development
  • Extensive experience of flow cytometry
  • Knowledge of a range of platforms for high sensitivity immunoassay development, which may include Singulex, MSD etc. would be an advantage
  • Experience working with a range of internal stakeholders including Research Scientists, Non-Clinical Safety and Translational Medicine
  • An ability to represent the department in project teams to ensure bioanalytical data generated is of the highest quality
  • An understanding of pathology and therapies underlying immunological and neurological disease would be an advantage
  • Provide day to day delivery of in house flow cytometry in support of the company’s biomarker strategy and projects
  • Provide additional immunoassay support as appropriate
  • Support the development and maintenance of state of the art technologies
  • Provide the appropriate levels of biomarker verification and assay quality
  • Deliver critical data in a timely manner to the project teams
  • Troubleshoot technical issues and providing solutions, which may arise during the course of assay development and / or sample analysis
  • Well organized, capable of communicating clearly to partners and stakeholders
  • Liaise with other experts (e.g. statisticians) to design appropriate experiments
  • Contribute to the preparation and review of appropriate reports and documentation
214

Senior Scientist Resume Examples & Samples

  • Indirectly managing laboratory technicians
  • Organising release and stability analyses
  • Designing experiments
  • Performing release and stability testing in the laboratory
  • Preparing documentation (procedures, protocols, reports, methods)
  • Verifying data
  • Following deviations and incidents
  • Validating results within LIMS system
  • Presenting/discussing results in project team meetings
  • Actively representing the team in project teams
  • Providing analytical support to business partners as appropriate (e.g. RA, QA, QC)
215

Senior Scientist Resume Examples & Samples

  • Conduct final review of documentation
  • Write, update and evaluate new test methods, SOPs, LPMs, using USP, NF, method validation
  • Coordinate testing/direction of the laboratory (non-supervisory role)
  • Assist in administrative functions
  • Train other analysts in laboratory techniques
  • Perform routine microbiological testing of all samples
  • Perform routine testing to support other departments
  • Calibration/validation of instrumentation
  • Represent department on project and cross-functional teams and committees
  • Follows Teva Safety, Health, and Environmental policies and procedures
  • Performs other duties as assigned or as business needs require
  • Documentation and microbe reviews completed within timelines and are complete and accurate
  • Validation packets are reviewed and any issues resolved in timely manner
  • Research notebooks and identifications are evaluated and reviewed in a timely manner
  • Procedures are complete, accurate, understandable and up-to-date
  • Projects are coordinated and completed in a timely manner
  • Excellent organizational skills and attention to detail, self-driven and motivated
  • Excellent computer skills including MS Office, Windows and LIMS
  • Excellent at multitasking, handling multiple projects at one time, and changing priorities based on business needs
  • History of significant contribution to cross-functional teams and projects
  • History of significant project management role on cross-functional teams and projects
  • Specialized or Technical
  • Working knowledge of Microbial Limits Testing and identification procedures and/or other microbiology methods, and proficiency in most of these techniques
  • Excellent knowledge of FDA, USP, ICH, cGMP, and cGLP requirements in a pharmaceutical quality control laboratory
216

Senior Scientist Upstream Development & Operations Resume Examples & Samples

  • Demonstrated experience with the development, scale-up and tech transfer of upstream processes for clinical or commercial manufacturing of biologics
  • Demonstrated experience in mammalian cell culture process characterization and scale-down model development with good understanding of product quality attributes
  • Hands-on experience in development of cell culture media & feeds for fed-batch and/or perfusion processes
  • Deep knowledge base in biological and engineering principles used for production of recombinant proteins & antibodies from mammalian cells including molecular biology, cell biology, cell metabolism, upstream process optimization and scale-up
  • Track record of scientific contributions in the field of upstream process development through publications and presentations
  • Demonstrated ability to lead functional teams in multidisciplinary environment
  • Experience in applying advanced data analysis techniques (e.g. multivariate data analysis) and computational tools (mathematical models) for use in process monitoring and/or control (e.g PAT)
  • Experience in metabolic modeling and associated experimental techniques (metabolic flux analysis, analytical methods)
  • Experience in applying Omics technologies ( transcriptomics, metabolomics, proteomics) for process understanding and/or optimization
  • Solid understanding and experience in cGMP manufacturing of biologics
  • Authoring/reviewing experience with regulatory filings of biologics in US or worldwide
217

Formulation Senior Scientist Resume Examples & Samples

  • Provide effective leadership for short term project teams addressing manufacturing and formulation
  • Promote and support application of QbD principles for identification and control of critical process parameters (CPP)
  • Serve on co-development teams to provide Global Manufacturing Supply (GMS) manufacturing expertise and input with regard to preferred process technologies and specifications
  • Support product transfer teams to provide GMS manufacturing expertise and to identify and mitigate quality and supply risks related to drug product manufacturing
  • Develop and maintain relationships with colleagues within GMS and VMRD network to identify potential value-creating opportunities for process improvement and scrap reduction
  • Facilitate the flow of sufficient information from all sources to fully understand customer needs, and follow up to assure business requirements are fully met
  • Undertake complex troubleshooting and problem solving activities
  • Keeps abreast of technological advances specific to drug product manufacturing, applying new techniques and methods where appropriate
  • Comply with all safety and quality policies and requirements. Assure that the laboratories maintain a safe and clean working area. Follow cGMP procedures
  • BS degree in chemistry, or chemical engineering is required. Masters degree preferred but not required
  • 10 years of industry experience, minimum of 5 years hands on experience in the development and manufacture of medicated feed additives
  • Mastery of scientific principles, practices and theories with broad process and analytical experience
  • Familiarity with commercial scale MFA equipment and processes
  • Demonstration of strong skills in manufacturing formulation processing, development and optimization
  • Familiarity with operational effectiveness and lean principles, Green/black belt certification preferred but not required
  • Ability to work closely and communicate with operations colleagues to solve production issues
  • Foster a productive environment that encourages teamwork and commitment to results
  • Demonstrated capability to effectively apply knowledge, lead multiple activities and balance priorities
  • Willingness to travel occasionally, including international travel, as needed (~25%)
218

Senior Scientist Resume Examples & Samples

  • Independently research and proposes novel analyte candidates and new technologies needed to achieve the desired product profiles
  • Produce and characterize analytes needed for test development
  • Develop and validate immunochemistry-based diagnostic tests
  • Design and conduct diagnostic feasibility, optimization and regulatory studies
  • Draft product development related documentation including Development Study Reports, Outlines of Production, transfer documents as well as field study protocols and reports
  • Transfers developed products to manufacturing
  • Lead one or more diagnostic projects from concept to approval or launch, including the project planning to maintain timelines
  • Mentors and assists junior colleagues
  • MSc in microbiology/immunology/biotechnology or related discipline with a minimum of 10 years of demonstrated work experience, including 5 years of assay development experience
  • PhD in microbiology/immunology/biotechnology or related discipline with a minimum of 3 years of demonstrated work experience, including 2 years of assay development experience
  • A track record of success in a matrix research organization, e.g. know how to leverage all the resources available, even those outside your line, to accomplish your goals
  • Outstanding problem solving and excellent experimental design skills
  • Ability to work efficiently and independently
  • A good understanding of regulatory considerations in the diagnostic space
219

Senior Scientist Resume Examples & Samples

  • Contribute to the development and support of new target animal disease models and efficacy and safety studies by
  • Suitable candidates will have a DVM/VMD from an accredited College of Veterinary Medicine and a minimum of 3 years of experience in swine and/or cattle medicine, swine and/or cattle infectious disease, or swine and/or cattle immunology
  • Must also be a creative/independent thinker with a desire to investigate problems and to utilize a team to create innovative animal models
  • Licensed to practice in at least one state with the expectation to become licensed in Michigan
  • Federally accredited
  • Ability to communicate and interact effectively with colleagues as a participant on multi-disciplinary teams
  • Strong hands-on expertise in a range of livestock techniques including handling, restraint, dosing, venipuncture, clinical examination and diagnosis, minor surgical procedures and necropsy
220

Senior Scientist Resume Examples & Samples

  • Design and conduct studies to identify and evaluate potential new companion animal veterinary medicines
  • Independently evaluate appropriate medical literature, create clinical assessment tools, identify and acquire appropriate technology and design and implement relevant models to assess therapeutic approaches
  • Development of appropriate protocols, the planning and scheduling of studies, the organization and management of scientific data, and the timely presentation of scientific results
  • Participation in and coordination of studies conducted by outside collaborators or in collaboration with academic institutions
  • Train/mentor scientists and technicians
221

Senior Scientist Resume Examples & Samples

  • Provide effective leadership for short term project teams addressing process and chemistry issues
  • Serve on co-development teams to provide GMS small molecule chemistry expertise and input with regard to preferred process technologies and specifications
  • Support product transfer teams to provide GMS small molecule chemistry expertise and to identify and mitigate quality and supply risks related to process chemistry
  • Conduct or coordinate laboratory experiments to generate analytical results. Collect and analyze technical data, generate reports including conclusions and recommendations where needed
  • Help coordinate synthesis of global Zoetis reference standards using internal and external resources
  • Possess broad understanding of analytical technologies, concepts and principles, particularly HPLC
  • Collaborate and contribute general analytical support to GMS global analytical team colleagues
  • Keeps abreast of technological advances specific to process refining techniques, applying new techniques and methods where appropriate
  • BS degree in chemistry, or chemical engineering is required
  • 10 years of industry experience, minimum of 5 years of process chemistry experience
  • Mastery of scientific principles, practices and theories with broad analytical experience
  • Familiarity with commercial scale equipment and processes is desired
  • Demonstration of strong skills in organic and analytical chemistry
  • Skilled in applying statistical methods to analytical method performance characteristics
  • Effective interpersonal skills. Demonstrated ability to work effectively in cross functional and culturally diverse work environment. The ability to confidently assert a technical position in the face of opposition
  • Strong understanding of regulatory and quality requirements
  • Proven record of consistent performance
  • Commitment to delivering results
  • Ability to develop, execute and report experiments, studies and projects
  • Demonstrated excellence in planning and organizational skills
  • Comprehensive demonstrated skills in communication (oral and written) – particularly technical writing
222

Senior Scientist Resume Examples & Samples

  • Providing leadership in the identification, development, and deployment of continuous manufacturing technologies to support drug substance process development and commercialization. Specific areas of focus include: reaction engineering/catalysis, separations, crystallization, distillation, automation and integration of engineering unit operations, and on-line chemical analysis. Champion deployment and adoption of advanced processing methodologies and train other scientists and engineers in their use
  • Supporting batch and continuous drug substance process development via laboratory experimentation, pilot scale demonstration, drug supply preparation, management of external scientific activities, and technology transfer to third party manufacturing sites
  • Defining, developing, and demonstrating commercially viable batch and continuous organic syntheses for the manufacture of small-molecule advanced intermediates and active pharmaceutical ingredients
  • A Ph.D. degree with 5+ years of academic, post-doctoral or pharmaceutical industry experience; an MS degree with 8+ years of pharmaceutical industry experience; or a BS degree with 11+ years of pharmaceutical industry experience. Degrees with a life science or engineering concentration required, with a preference for concentrations in chemical engineering or chemistry
  • A demonstrated understanding and working knowledge of chemistry and chemical engineering fundamentals; advanced technical knowledge and experience in API process development, process scale-up, troubleshooting, and optimization; applied kinetics, thermodynamics, and transport fundamentals; as well as familiarity with modern laboratory instrumentation (HPLC, GC, FTIR, Raman, FBRM, DSC, TGA, XRPD, etc), and laboratory/plant implementation of PAT
  • Experience with modeling complex, physicochemical systems; data analysis; statistical design of experiments; QbD concepts, and fluency with common physical property and process modeling tools (Aspen, Dynochem, Matlab, etc.). Familiarity with laboratory/process automation
  • A track record of successful laboratory/pilot-scale development and modelling in the areas of reaction engineering, catalysis, crystallization, separation technologies, and drying
  • The ability to successfully interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; chemical engineers, project team members; and manufacturing personnel
  • Experience with the management of external scientific activities and CRO/CMO relationships
223

Senior Scientist Resume Examples & Samples

  • Directly accountable for bioassay development for early and late stage development programs, development of fit-for-purpose biological characterization assays, assay qualification/validation, and strong collaboration with stakeholders in partner organizations. Inspires innovation and operational excellence and fosters a continuous learning environment. Responsible for sound scientific strategy to support regulatory acceptance of biological assays and specifications in clinical development. Translate strategy into actionable objectives, and anticipate and address technical, regulatory, and other business needs. Role may offer opportunities to manage and lead an analytical CMC team
  • Typically 4-6+ year’s directly applicable experience in biopharmaceutical development
  • Strong history of rigorous science applied to drive technical accomplishments
  • Understanding of regulatory and industry guidelines in the area of potency assay development
  • Strong mechanistic understanding of biotherapeutics required
  • 1603743
224

Senior Scientist Resume Examples & Samples

  • The successful candidate is expected to be a strong experimentalist that can lead independent research, with extensive cell molecular biology and tissue culture experience
  • Take a scientific leadership position and work productively in a fast paced results oriented interdisciplinary team environment
  • Effective oral and written communication capabilities
  • A bioinformatics background using software packages and statistically oriented languages is highly desirable
  • Have a PhD with at least 4-8 or more years of industrial experience or equivalent
  • 1603647
225

Senior Scientist / Technology Leader Resume Examples & Samples

  • Develop algorithms, software and applications in areas such as Visual Security & Surveillance, Autonomous Robotics, and Video Data Mining
  • PhD in Computer Science/Electrical Engineering or related fields with a focus on Computer Vision
  • 6-8 years experience in creating and executing on projects funded by external agencies such as DARPA, ONR, AFRL, DHS, DTO and other government R&D and commercial agencies is preferred
  • Given the nature of US Govt. business in this area, US Citizenship/Permanent Residency is preferred, and US Govt. Clearances are preferred. Exceptional candidates will be considered even if they do not have permanent residency
  • O Navigation, GPS-denied localization
226

Senior Scientist / Seasoning Resume Examples & Samples

  • Responsible for Seasoning Strategy
  • Develop a plan for creating and managing the Food Seasoning Group
  • Accountable for developing formulas for Marinades, Side Dishes, Sauces & Gravies, Batter & Breaders and other Seasoning applications
227

Senior Scientist / Bar, Cereal Resume Examples & Samples

  • Will require some travel to customers
  • Strong presentation skills and the ability to rapidly develop a relationship with internal and external customers
  • Responsible for Cereal and Bar Strategy
  • Accountable for developing formulas for cereal, bars and granola applications
  • Responsible for maintaining customer relationships
228

Senior Scientist Resume Examples & Samples

  • At least 3-5 years working experience in analytical lab
  • Master degree in Analytical Chemistry, Applied Chemistry or equivalent
  • Practical and theoretical knowledge in spectrometry (i.e. FTIR, NMR and UV-vis)
  • Preferably knowledge and experience with chromatography, such as LC/MS, GC/MS and HPLC
  • Ability to present results comprehensively in reports and oral presentation
  • Be familiar with instrument maintenance and qualification
  • Good organizational skills required to react flexibly to varying assignments and different customers
  • Good communication skills required in dealing with team members, customers and colleagues from other departments and sites
  • Good ability to communicate effectively in both oral and written English
229

Senior Scientist Resume Examples & Samples

  • Bachelor degree in Organic, analytical or bioorganic chemistry or equivalent with at least 2 years’ experience with strong analytical chemistry background
  • Ability to operate and interpret chromatography, such as HPLC, GC, GPC, LC-MS and GC-MS, etc. Be familiar with laboratory equipment maintenance, calibration and qualification etc
  • Good English proficiency in both oral and written
  • Excellent PC skills
230

Senior Scientist Resume Examples & Samples

  • PhD in Chemical Engineering, Chemistry, Polymer Chemistry or Materials Science and 2+ years of industrial experience in small molecule synthesis or polymer synthesis or Master's degree in Chemical Engineering, Chemistry, Polymer Chemistry or Materials Science and 5 years of industrial experience in small molecule synthesis or polymer synthesis required
  • Familiarity with the BASF Innovation process
  • Experience with writing project proposal and getting them approved
  • In-depth know-how about the synthesis and structure-property relationships of Amphiphilic Systems required
  • Familiar writing project proposal and getting them approved either in an academic or industrial organization
  • Has in-depth know-how about the synthesis and structure-property relationships of Amphiphilic systems
  • Ideally experience in one of the applications fields of Home Care, Personal Care, Oilfield & Mining Chemicals or Fuel Additives & Lubricants
  • Excellent communication and networking skills
  • Willingness to learn and improve
  • Strong skills in researching literature and communicating technical concepts in verbal and written form
231

Senior Scientist Resume Examples & Samples

  • Develop commercially viable products in a timely fashion
  • Plan and conduct a variety of complex technical projects under very general directions
  • Perform work independently with instructions as to the general results expected
  • Participate in technical and business strategy development
  • PhD or MD / Chemist/Chemical Engineer experience requested
  • Research activity for Wet cleaning and Wet etch technology preferred
  • Proficiency in electro-chemistry including electrochemical physical property measurements, skilled in wet etching a plus
  • Develop innovative approaches to solving complex problems
  • Familiar with chemical and technical literature
  • Research literature to understand past developments and to facilitate the development of original strategies
  • Identify industry trends in order to invent and develop novel and patentable chemistry and/or processes
  • Independently design / conduct experiments and effectively analyze the results of experiments
232

Senior Scientist Resume Examples & Samples

  • Ph.D. or equivalent in biology, biochemistry, analytical chemistry, or a relevant scientific discipline, with 6 or more years of industry or relevant experience
  • Candidates with Bachelor’s or Master’s degrees will be considered with the appropriate experience
  • 1603717
233

Senior Scientist, Drug Substance Development Resume Examples & Samples

  • Key member of a dynamic, scientifically driven team dedicated to the discovery and development of elegant chemical syntheses and processes for active pharmaceutical compounds
  • Serve as Drug Substance Development representative on multidisciplinary CMC teams
  • Manage technology transfers to and manufacturing of GMP Drug Substance at Contract Research Organizations
  • Keep current with required GMP training and qualifications
  • Evaluate and maintain safety, regulatory, and compliance standards as they relate to the development of pharmaceuticals
  • Supervise scientists under a project specific matrix organization
  • Ph.D. in Organic Chemistry with 5 + years relevant industrial experience
  • Experience in pharmaceutical development as it relates to route selection, process development, salt selection, polymorphism, solubility, and stability testing
  • Proven track record in developing and scaling-up innovative, safe and effective processes for the manufacture of chemical intermediates and solutions to overcome synthetic and manufacturing obstacles
  • Strong interpersonal skills and the ability to work in a fast paced, multidisciplinary team environment. Ability to work independently or in team environments under deadlines. Verbal and written communication skills are essential
  • Experience with CMC issues encountered in drug development is highly desirable
  • Familiarity with GMP manufacturing and IND/NDA filings is a plus
234

Senior Scientist Resume Examples & Samples

  • Design, execute and lead independent research supporting project goals including developing novel methodologies, protocols and or test procedures that contribute to research goals
  • Contribute to new drug proposals
  • Direct and oversee experimental design and results of scientists
  • Actively participate in multiple cross functional teams/initiatives and external collaborations
  • Independently communicate results/updates of scientific programs in context of overall project goals to senior level management. Prepare clear technical reports and publications
  • Develop expertise in a specific project relevant area or technology. Interpret the current literature while keeping abreast of project relevant publications
  • Comply with all applicable regulations. Demonstrate fiscal responsibility and ensure that work performed in area of responsibility is conducted in a safe and compliant manner. Maintain proper records in accordance with SOPs and policies
235

Senior Scientist Resume Examples & Samples

  • Conduct a real-time flow cytometry assay in support of increased manufacturing process control and consistency in viral growth kinetics
  • Development of new analytical technologies to be used in vaccine manufacturing
  • Participate in the transfer of process analytical technologies (PAT) to cGMP manufacturing facilities, and support implementation and operations in the new PAT laboratory
  • Support routine laboratory operations, including the coordination of scheduling activities, cleaning, supply ordering, and preventative maintenance
  • Support proactive process monitoring through assay and process data collection, GMP laboratory experiments (e.g., viral growth curves), etc
  • Characterize existing processes, identify key sources of variability, and identify potential process improvements
  • Conduct laboratory experiments to support technical investigations and implement sustainable long term solutions
  • The ability to work a flexible, rotating shift schedule, which will include nights and/or weekend coverage, will be required based on manufacturing process support needs
  • BS in life science (e.g., biology, microbiology, immunology, virology, etc.), or engineering (e.g., biomedical, chemical). Must have excellent communication, documentation, and interpersonal skills; as well as strength in data analysis/interpretation, and the ability to exercise scientific judgment and for real-time decision-making
  • Must be willing to be vaccinated and achieve, and/or blood tested for titer against the Varicella (chickenpox) virus
  • Minimum 2 years of experience in a relevant industry or MS in life science or engineering
  • Experience with flow cytometry and/or performing immunoassays is preferred
  • Experience in analytical testing utilizing a variety of biochemical, molecular, and cell biology techniques. Experience in laboratory operations including GMP documentation, equipment maintenance, and scheduling
  • Experience with cell culture and aseptic techniques
236

Temporary Senior Scientist Resume Examples & Samples

  • Air and underwater acoustics
  • Structural acoustics and vibrations
  • Active noise and vibration control
  • Finite-Element Analyses (FEA) and Statistical Energy Analyses (SEA)
  • Advanced modeling and simulations of physical systems
  • Outstanding record of technology innovation and leadership
  • Demonstrated excellence in interacting with customers and decision-makers
  • Proven track record in writing successful proposals,standing up research teams,executing projects successfully
  • BS, MS, or PhD with 6-11 years of experience. Advanced degree preferred
237

Senior Scientist, Biophysics Lead Discovery Resume Examples & Samples

  • Lead the design and implementation of screening strategies that reflect the pharmacology to be modulated in subsequent hit-to-lead discovery programs
  • Provide scientific leadership to a team that (1) develops biophysical assays such as SPR, thermophoresis, ITC and mass spectrometry for hit validation and fragment screening (2) executes assays to validate HTS hits (3) analyzes data including presentation at program team meetings
  • Develop innovative approaches to hit triage and fragment screening including evaluation of new technologies
  • PhD in biochemistry, biophysics or related areas is required
  • At least 4 years of industry experience in biophysical assay development for the characterization of small-molecule interactions with proteins is required
  • Expertise with detection methods (ie: SPR, thermophoresis, ITC and mass spectrometry) is required
  • Hit triage experience is preferred
  • Expertise in cardiovascular, immunology, infectious diseases, neuroscience or oncology therapeutic areas is preferred
  • Experience working with and guiding external collaborators in industry or academia is preferredR&D
238

Senior Scientist Resume Examples & Samples

  • Translate market needs into novel materials and chemistries. Develop, implement and generated analytical solutions to automotive coating performance problems
  • Innovate, develop and commercialize novel material and chemistries to service the future needs of the market
  • Develop hypotheses and root causes based on sound scientific principle and utilizing associated scientific methods whether these are founded in chemistry, physics, material, analytical or other disciplines
  • Ph.D. Degree in Chemistry, Material Science, Chemical Engineering or a Non-Chemical Science and 5 years of industrial experience developing and formulating coatings or adhesives for automotive applications, industrial coatings, protective coatings, marine coatings, base coat or clear coat required OR Masters Degree in Chemistry, Material Science, Chemical Engineering or a Non Chemical Science and 7 years of industrial experience developing and formulating coatings or adhesives for automotive applications, industrial coatings, protective coatings, marine coatings, base coat or clear coat required OR Bachelor's Degree in Chemistry, Material Science or Chemical Engineering with 10 years of industrial experience developing and formulating coatings or adhesives for automotive applications, industrial coatings, protective coatings, marine coatings, base coat or clear coat required
  • Related experience should include the development of coating systems designed for applications similar to those used in the Automotive industry, but may not be specific to Automotive OEM. Experience in Industrial or specialty markets may be applicable, but will depend upon knowledge and breath of chemistry
  • Experience and breadth in chemistries used in coatings, should include those relating to multiple paint systems and coating layers. i.e. Electrocoat, Primers, Topcoats (Color and Clearcoat)
  • Direct customer experience is a plus Knowledge/Skills
  • This position requires strong business acumen, as it is expected that contributions are made in the developing of technology strategies for the Automotive OEM coatings industry, as well as new business development including new markets
  • Good managerial and Project Management skills communication skills are required
239

Senior Scientist, Product Development Resume Examples & Samples

  • B.S. or M.S. with 3-5 years of experience is required. Experience in consumer foods or beverage industry is preferred. Food Science degree is preferred
  • Understanding of Product Development techniques including formulation, stability testing, product/package interaction, sensory and consumer testing
  • Basic technical understanding of ingredient functionality and process technology for application in new product development
  • Able to analyze complex data to make clear technical recommendations
  • Able to manage multiple projects, priorities, and deadlines
  • Experience in juice or beverage product development a plus
  • Able to handle a fast paced and constantly changing work environment
  • Familiarity with functional nutrition food and beverage trends a plus
240

Senior Scientist Resume Examples & Samples

  • Primary Accountabilities / ResponsibilitiesKey statements which describe the major accountabilities or responsibilities and the expected end result
  • · Educated to at least degree level in a scientific subject and/or appropriate post graduate qualifications
  • · Strong knowledge of statistical theory and its application to sensory/consumer research
  • · Personal leadership qualities
  • · Adherence to time scales
  • · Strong written and verbal communication
  • · Demonstration of proactivity
  • · Proven ability to work independently
  • · Develops and adapts action plans as needed to deliver the bottom line and long term strategic goals
  • · Communications are tailored to audience and recommendations and are recognized as delivering against business goals
  • Practical experience of application of statistical analysis
  • Interest in food
  • Expierence with a category appraisal studies
241

Senior Scientist Resume Examples & Samples

  • This role would drive the completion and improvement of the breast menu offering from Leica Advanced Staining. This role would directly interact with other key function such as Regulatory Affairs, Clinical Affairs, Product Management and Operations. Not all of these functions will be based at Newcastle so the ability to communicate and effectively cooperate with functions in different parts of the globe is essential
  • To provide technical leadership and mentoring support to projects; develop, plan, execute and report experiments to drive the development of robust IVD assays, ensuring that delivery of the project to business is within budget and on schedule. This may also require a comprehensive literature search, a review of existing/rival products, and use of databases prior to deciding which approach to use
  • To ensure that Design Control is rigorously adhered to and applied to all development projects
  • To ensure that opportunities for continuous improvement, achieved via DBS, are identified
  • Acting as part of a team, or as a project lead, to examine the viability of potential research projects
  • Microscopic slide examination and interpretation of antibody/probe staining primarily on formalin fixed paraffin embedded tissue where required
  • Participation in technical support and customer complaint investigations, when requested
  • 3-5 years previous experience in IVD development – ideally acting as a project lead. Experienced in relevant/appropriate scientific domain
  • Previous experience within a regulated environment and deep understanding of Design Control
  • Experience and understanding of histopathology and immunohistochemistry
  • Understanding of in situ hybridisation (FISH and CISH)
242

Senior Scientist Resume Examples & Samples

  • Design, plan, perform, interpret and document DS/DP related analytical activities including release/stability testing, method development/validation etc. under minimal guidance from more experienced team member
  • Provide scientific and technical guidance. Coach team members as needed. 9.Interact/collaborate with other groups/functions to facilitate transfer of knowledge of DS/DP
  • Give guidance to team members and work according to appropriate SOP’s, GLP, GMP, OQM, HSE, ISEC and Novartis guidelines
  • Contribute to risk analyses and/or peer review and process challenge meetings
  • Generate scientific documents to hand over to internal and/or external partners and actively support generation of international registration documents under adequate guidance from more experienced team members. 16.Actively contribute to team goals
  • Report and present scientific/technical results internally and contribute to publications, presentations and patents
  • Evaluate new lab equipment and prepare CAR and URS if applicable 19.Contribute to maintenance of infrastructure/equipment and required investments
243

Senior Scientist Resume Examples & Samples

  • Serve as technical expert for the department and as required to meet corporate goals
  • May provide supervision, guidance, and direction to lower-level technical/scientific staff
  • It is the responsibility of each employee to work in a safe and responsible manner in order to create an injury-free and incident-free workplace
  • Comply with all job-related safety and other training requirements
  • Bachelor's degree with 4+ years' related experience
  • Experience with LYOPHILIZATION required!
244

Senior Scientist Resume Examples & Samples

  • PhD, preferably in microbiology, immunology or cell biology
  • OR Masters degree with 2+ years of relevant experience
  • OR Bachelor's degree with 4+ years of relevant experience
  • Experience in developing cellular and immunologically based assays strongly preferred
  • Direct hands-on experience in quantitative and qualitative analysis using a variety of immunochemistry platforms and/or cell based culture, assay and/or staining (Fluorescent microscopy, FACS) is expected
  • Strong foundation of knowledge in biological sciences and good aseptic technique is required
  • Good verbal and written communication skills are expected
  • Ability to develop analytical methods to meet international system suitability expectations is expected
  • Demonstrated working knowledge of ICH and USP guidelines and FDA GMP regulatory requirements is desired
245

Senior Scientist Resume Examples & Samples

  • Ph.D. in Industrial Pharmacy, Materials Engineering or related field with significant experience in spectroscopy
  • Masters degree in Industrial Pharmacy, Materials Engineering or related field with significant experience in spectroscopy and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable 4+ year) or equivalent combination of education, training, & experience
  • Knowledge of general chemistry and separation science
  • Possess strong mathematical and problem solving skills
  • Demonstrated ability to develop and document scientific findings
  • Proven troubleshooting abilities
  • Willingness to share knowledge and grow in the field of PAT as it relates to pharmaceutical applications
246

Senior Scientist Resume Examples & Samples

  • Master's Degree in Polymer Chemistry, Material Science or Chemical Engineering from an accredited university with 5+ years of related work experience
  • Good knowledge in resin structural property relationship
  • Good knowledge in thermoset resin processing, properties and applications
  • Independence, creativity, initiative, and results-oriented
  • Hands on experience in operating lab equipment
  • Experience with thermal analysis, rheology and mechanical testing equipment (e.g. Instron)
  • Prior experience with Structural Composite applications is required
247

Senior Scientist Resume Examples & Samples

  • Perform product transfer efforts
  • Work within the established design control process for product development and to transfer new products from R&D into manufacturing
  • Understanding of the commercial value of the work
248

Senior Scientist Resume Examples & Samples

  • Full knowledge of all data generation and statistical programs
  • Full understanding and knowledge of separation science and general chemistry
  • Proficient in operation and troubleshooting of a wide variety of analytical instrumentation and data acquisition systems
  • Full understanding of cGMP requirements, PPD & client SOPs, ICH guidelines, USP requirements and FDA guidance
  • Proven analytical problem solving abilities
  • Ability to manage multiple tasks and priorities for successful project completion
249

Senior Scientist Resume Examples & Samples

  • Developing the manufacturing site execution plan per product, in line with the overall strategy and plan as outlined by the PDMS/ API sub-team and JSC New Product Team. The TLI will ensure alignment and endorsement of this strategy within the manufacturing site and TLI function
  • Providing required manufacturing technical support, document technical input, review and approval and serving as the JSC technical expert for the product
  • Coordinating all site related technical and regulatory documents and API technical support
  • Partnering with the DS TI to provide all DS manufacturing site related needs to the API Subteam as the single point of contact for all site DS issues
  • Driving and assuring manufacturing site readiness and execution in partnership with the site functions and management, supply chain technical functions (platforms/engineering), API TI, NPL, and DS TLI functional lead and SME’s
  • Delivering clinical DS materials through commercial DS supply from the manufacturing site, meeting manufacturing performance, cost, and process robustness requirements, in line with QbD principles and supply chain performance metrics
  • Planning and execution of DS TLI and manufacturing site project deliverables ensuring delivery of agreed milestones and objectives
  • Coordinating and executing product introduction along the project continuum from DS transfer through launch (responsibilities for launch planning/logistics out of scope) and providing commercial support of the product where appropriate
  • Optimizing the new product introduction process, making use of JSC technology platforms, accelerating development timelines, streamlining the technical transfer process, and technical implementation of QbD
  • A bachelor’s degree in Chemistry, Pharmaceutics, Engineering, or related area. A minimum with 5-10 years of experience in pharmaceutical development or pharmaceutical manufacturing is required
  • Knowledge of both pharmaceutical product R&D and/or Technical/Site Operations functions and experience with large molecule drug product processes and manufacturing is required
  • Motivated, self-starter able to work independently with demonstrated problem solving skills.R&D
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Senior Scientist Resume Examples & Samples

  • Planning and execution of experiments and analysis or interpretation of the results following GLP
  • Effectively communicate project progress and issues/risks to manager
  • Assist in the maintenance of laboratory facilities, equipment and consumables
  • Contribute to the continuous improvement of processes and procedures at LBS
  • Support production where required
  • Compliance to international quality standards
  • Achieve best practise safety performance levels
  • A tertiary qualification in a relevant science discipline, eg. biochemistry, biology, chemistry
  • The ability to work effectively towards deadlines
  • A positive attitude along with the desire to learn and develop
  • The ability to communicate scientific ideas and concepts to audiences with and without technical knowledge
  • Problem solving and technical troubleshooting skills
  • Experience in a Histology laboratory