Senior Associate Scientist Resume Samples

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PG
P Green
Price
Green
719 Paula Lock
Phoenix
AZ
+1 (555) 218 2737
719 Paula Lock
Phoenix
AZ
Phone
p +1 (555) 218 2737
Experience Experience
Philadelphia, PA
Senior Associate Scientist
Philadelphia, PA
Welch-Luettgen
Philadelphia, PA
Senior Associate Scientist
  • Overseeing laboratory activities including scheduling, equipment maintenance, and vendor communication
  • Support raw material investigations and life cycle activities related to raw materials including leading and/or participating in root cause analyses
  • Serve as an independent contributor to developing and implementing new methods and technologies, including flow cytometry applications
  • Initiating and leading new technology assessment including external collaborations
  • Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines Performs method validation following protocol
  • Take an active role in designing experiments and testing hypotheses in collaboration with multiple team members and teams within the division
  • Develop and execute bioanalytical assays, including LC-MSMS and ligand binding assays (LBA), for PK and exposure assessment of biotherapeutics
Phoenix, AZ
Senior Associate Scientist, Immunology
Phoenix, AZ
Bogisich Inc
Phoenix, AZ
Senior Associate Scientist, Immunology
  • Plan and execute scientific experiments
  • Maintain well written and accurate research electronic notebook detailing work undertaken
  • Design, plan, and execute cell based assays and troubleshoot existing protocols with guidance
  • Works independently
  • Provides input into experimental designs
  • Execute experiments independently
  • Maintain primary and cancer cell lines and conduct routine cell culture tasks
present
Dallas, TX
Senior Associate Scientist Pdms Lm-ad Cork
Dallas, TX
Will and Sons
present
Dallas, TX
Senior Associate Scientist Pdms Lm-ad Cork
present
  • Write SOP’s, protocols, work instructions and training modules
  • Customer focus and results and performance driven
  • Supports troubleshooting and manages laboratory investigations
  • Lead continuous improvement projects
  • Participates in Technical discussions with with LM-AD Method development group
  • Testing to support assay validation/qualification and other studies
  • Support the maintenance of a GMP compliant laboratory
Education Education
Bachelor’s Degree in Chemistry
Bachelor’s Degree in Chemistry
California State University, Northridge
Bachelor’s Degree in Chemistry
Skills Skills
  • Strong written and verbal communication skills, good interpersonal skills, ability to multi-task, and a strong desire to learn, contribute and collaborate
  • Excellent interpersonal & collaborative skills with an ability to operate as part of a team in highly inter-dependent environment is critical
  • Capability to pay attention to details, stay focused on key objectives, and deliver high quality data in a timely and well organized manner is desired
  • Ability to work independently or in a team under deadline. Strong verbal and written communication skills are essential
  • Strong organic laboratory skills and knowledge of organic synthesis
  • Ability to independently generate precise, reliable data and skillfully analyze the data is essential
  • Strong interpersonal skills and the ability to work in a fast paced, multidisciplinary, matrixed environment
  • Demonstrate the ability to analyze and present data in professional 'publication ready' format
  • Exhibits sound scientific judgment based on reasonable assumptions and available information
  • Demonstrate clear and professional verbal and written communication (excellent presentation skills)
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15 Senior Associate Scientist resume templates

1

Senior Associate Scientist Resume Examples & Samples

  • Bachelor's degree in Biology, Chemistry, Pharmacology or other relevant scientific field, with at least 4 years of industry experience OR a Master's degree with at least 2 years of industry experience OR a PhD with relevant academic or industry experience is required
  • Experience in performing bioassays is required
  • Experience in immunochemical techniques, including flow cytometry and immunoassays or nucleic acid assays is required
  • Experience with method development in a variety of cell-based bioassays and binding assays is required
  • Experience with automation, liquid handling or high-throughput analytical technologies is preferred
  • Experience in molecular biology, gene construct design and molecular cloning, reporter gene assays and engineering stable cell lines to support cell based assay development would be desirable
  • Experience with gene therapy and/or vaccines would be desirable.R&D
2

Senior Associate Scientist Resume Examples & Samples

  • BS degree in virology, molecular and cell biology, immunology or a related discipline with at least 10 years of hands on laboratory experience in a post graduate setting OR MS degree in virology, molecular and cell biology, immunology or a related discipline with at least 6 years of hands on laboratory experience in a post graduate setting OR. PhD in virology, molecular and cell biology, immunology or a related discipline with at least 3 years of hands on laboratory experience in a post graduate setting is required
  • Must be able to conduct innovative research experiments, including trouble shooting outcomes and proper controls, and designing follow on studies with minimal supervision
  • Must be able and willing to work with infectious agents
  • Familiarity with aseptic cell culture techniques is required
  • Hands-on experience and theoretical understanding of molecular biology techniques including cloning, transfection, PCR, reverse transcription and in vitro transcription is required
  • Hands-on experience to perform ELISA-based assays is required; immunoprecipitation studies, and Western blots are preferred
  • Hands-on experience and theoretical understanding of immunology techniques including thorough understanding of immune response pathways and ability to design immunological studies to understand effect and target of agonist is preferred
  • Must be able to operate basic and more advanced lab equipment including plate readers, cyclers, luminex, and automated robotic system
  • Prior experience with Southern and Northern blots are preferred
  • Proficiency in data analysis (excel, prism, lasergene or comparable applications) and presentation tools is required
  • Experience in drug discovery, assay development, and moving antiviral or immunomodulatory agents from discovery to clinical stage are preferred
  • Individuals with hands-on experience in HBV biology are preferredR&D
3

Senior Associate Scientist Resume Examples & Samples

  • Contributing to the ex vivo and in vivo studies for multiple research programs across the different stages of pre-clinical drug discovery
  • Design, execution and interpretation of in vivo studies for the validation and characterization of targets or therapeutic agents in the area of oncology and tumor immunology
  • Establish and perform in vivo model development, target inhibition, efficacy, mechanism of action, and pharmacokinetic/pharmacodynamics (PK/PD) biomarker studies, and will evaluate the influence of dose, schedule and therapeutic combinations in various cancer models
  • Demonstrate the ability to design, perform, interpret and utilize complex in vivo preclinical cancer models
  • Contribute to ex vivo analysis of tumor cells or immune cells by FACS, IHC and ELISA
  • Analyze and present data in a clear presentation ready format
  • Manage multiple in vivo experiments simultaneously
  • Contribute on various projects outside of his/her own, collaborate with stakeholders from all relevant functions, and keep up-to-date in the literature related to his/her field
  • Act as an expert resource on project teams, and demonstrate clear and professional verbal and written communication
  • Bachelor’s degree (B.S./B.A.) in biology, cellular and/or tumor immunology with at least 7 years of relevant pharmaceutical or biotech industry/lab/academic experience OR a Master’s degree (M.S.) with at least 5 years of relevant pharmaceutical or biotech industry/lab/academic experience is required
  • Experience with oncology relevant models - xenografts and syngeneic models are required; primary grafts, orthotopic models, transgenics or genetically engineered tumor models are preferred
  • Strong skills in tumor implantation techniques and dosing, proper handling of chemotherapeutics, tumor measurement, health monitoring, and data collection and analysis are required
  • Able to effectively present scientific data and concepts to colleagues and teams is required
  • Experience in writing drafts for IND filings is preferred
  • Experience presenting at external meeting is preferredR&D
4

Senior Associate Scientist Resume Examples & Samples

  • Good laboratory experience in both in vivo and in vitro settings is required
  • Extensive experience with generation of study cohorts through normal breeding and in-vitro fertilization, animal colony management, and deep understanding of transgenic animal models and behavioral endpoints is required
  • Previous experience with Compound Muscle Action Potential (CMAP) assessment or similar electrophysiological assay is highly desired
  • Prior experience working under BSL-2 and ABSL-2 containments is highly desired
  • Previous experience handling and dosing of animals including necropsies and intricate surgeries (including stereotaxic) in rodents is required
  • Prior experience with organizing, setting-up and executing complex in-vivo studies as well as the ability to learn new skills and to train employees is required
  • Previous management experience and strong interpersonal and organizational skills and commitment towards achievement of goals are required
5

Senior Associate Scientist, Research Resume Examples & Samples

  • Deep understanding of neurological cell models including ES/iPSC differentiation, handling of primary cells and routine cell lines
  • Strong background on cell-based assay development, HTS instrumentation and familiarity with automation
  • Demonstrated broad expertise in various cellular analytical methodologies including high content analysis, cell -based AlphaLISA, reporter cell lines, flow cytometry, and FRET/BRET
  • The candidate is expected to design creative scientific experiments and perform data analysis
  • Proficient use of Microsoft Excel, Powerpoint, GraphPad Prism, electronic notebooks (ELN)
  • Maintain ELN entries and data reporting to support medicinal chemistry
  • Comprehensive data analysis using state of the art software (e.g. Spotfire, Certara D360, Genedata Screener)
  • The successful candidate will be highly motivated with a demonstrated ability to successfully take on challenges, troubleshoot efficiently and quickly adapt to new responsibilities
  • The candidate must have excellent organization, oral and written communication skills
  • The ability to collaborate and work effectively as part of a team is essential
6

Senior Associate Scientist, Research Resume Examples & Samples

  • Must possess excellent expertise of rodent models of neurodegenerative diseases (preferentially PD-related models)
  • Must possess excellent surgical skills (stereotaxic injections), experience with handling, dosing of rodents, and collecting tissues (brain) and fluids (CSF, plasma)
  • Possess significant experience in immunohistological techniques, including tissue processing and sectioning, immunostaining, microscopy techniques and image analysis
  • Preferentially possess significant experience in a variety of biochemical analytical methods, including gel electrophoresis, Western blot, ELISA and protein extraction
  • Significant understanding of basic neurobiology of neurodegenerative diseases and mechanisms of neurodegeneration
  • Keen knowledge of experimental design, underlying scientific principles, and the ability to analyze and assess results
7

Senior Associate Scientist Resume Examples & Samples

  • Execute laboratory work plan / schedule developed with input from supervisor or senior team member
  • May draft technical documents such as methods or certificates of analysis
  • Performs parallel review of laboratory documentation and may become qualified to perform technical review of documents for accuracy, thoroughness and regulatory compliance
  • Trains others on procedures and laboratory techniques
  • Executes efficiency improvement project with guidance
  • Master’s degree and 0-2 years related experience
  • Bachelor's degree and 3-5 years related experience
  • Associate’s degree and >6 years related experience
  • Proactively address work issues at both an individual level and a team level
  • Able to prioritize and suggest alternatives or contingencies to achieve the correct technical solutions with most efficient resource utilization
8

Senior Associate Scientist Resume Examples & Samples

  • Develop and execute procedures or methods with high quality
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
  • Ability to identify aberrant/out of spec data and limited interpretation of data expected
  • Demonstrated ability to lead small team projects
  • Has applied knowledge of the principles and concepts of a discipline
  • Applies technical and functional knowledge to job related duties on most projects/ assignments within own group/project team
  • May contribute material to publications and/or external presentations
9

Senior Associate Scientist Resume Examples & Samples

  • Execute laboratory work plan / schedule developed with input from supervisor or senior team member. Sample types include in-process, release or stability. Techniques include HPLC, GC, Karl Fischer, Disintegration, Friability, Hardness, and appearance. Under direction, may perform method validation or transfer activities
  • Demonstrate leadership capabilities in a matrix environment
  • Bachelor's degree in chemistry or closely related physical science is required
  • 4-6 years of analytical chemistry experience is preferred
  • HPLC experience is preferred
  • GC experience is preferred
  • Wet chemistry experience is preferred
10

Senior Associate Scientist Resume Examples & Samples

  • Develop, optimize and validate state-of-the-art analytical methods for testing product quality and stability of biologic candidates
  • Perform analytical testing and characterization to support drug substance process development and
  • Provide technical support to QC and CRO testing laboratories
  • Write/review/approve protocols and reports, as required and based on experience
  • Demonstrated experience with the use of state-of-the-art analytical methods and biophysical characterization techniques for therapeutic proteins such as HPLC, CE and Spectroscopy
  • Demonstrated experience in analytical method development for release and stability testing of therapeutic proteins
  • Demonstrated experience in good documentation practices is essential
  • Experience in statistical experimental design and data analysis including Design of Experiments (DoE)
  • Proven ability to work effectively in team structures and collaborate with cross-functional internal/external partners
  • Willing to work in an environment where individual initiative, accountability, and professional integrity are required
11

Senior Associate Scientist Resume Examples & Samples

  • 1) Contributes to the development of priority drug candidates through the development, validation, and implementation of analytical methods involving modern analytical instrumentation including HPLC/UPLC, GC, dissolution, FT-IR, Karl Fischer titrations, etc
  • 2) Transfers validated methods to customer labs, including Celgene and partner-owned quality control (QC) labs
  • 3) Performs testing for development and clinical materials and stability samples in accordance with established methods, specifications and protocols with limited supervision
  • 4) Knows the fundamentals of analytical methodology and is able to troubleshoot instrumentation and method performance issues of moderate complexity
  • 5) Documents / reviews laboratory work using laboratory notebooks / worksheets that is detailed, timely and in compliance with GLP / GMP requirements
  • 6) Contributes to the preparation of high-quality technical reports as source documents for regulatory submissions
  • 7) Reviews data for compliance to specifications and acceptance criteria
  • 8) Communicates results according to project timelines and works with collaborators to understand project needs and contribute to overall analytical control strategy. Draws basic conclusions from data and results
  • 9) Other duties as assigned by supervisor
  • Minimum 5 years recent cGMP / GLP pharmaceutical laboratory experience, with in-depth knowledge of cGMP/GLP guidelines, ICH, FDA, and EMA guidances
  • Familiar with USP and other compendia
  • Extensive hands-on experience with separations techniques (HPLC, UPLC, GC, etc.)
  • Experience in laboratory investigation and documentation of OOS / OOT results
  • Strong verbal and written communication skills, and interpersonal skills as a team player
  • Willing to work in an environment where individual initiative, accountability to the team, and professional integrity are required
  • Recognizes analytical test problems, can investigate problems and take appropriate steps to resolve and communicate issues. Recognizes technological limitations and addresses them
  • Exhibits sound scientific judgment based on reasonable assumptions and available information
  • Demonstrated ability to conduct and document analytical laboratory experiments under minimal supervisory guidance
  • Experience in the development and performance of analytical tests for a variety of drug substances and products (including solid oral dosage forms and injectables) is a plus
12

Senior Associate Scientist Resume Examples & Samples

  • Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines
  • Performs method validation following protocol
  • Reports and resolves any unexpected issues under supervision
  • Performs method development under supervision
13

Senior Associate Scientist Resume Examples & Samples

  • Be a key member of the process engineering team that supports all of IPD’s process engineering efforts
  • Perform routine lab operations, execute experiment plan and monitor processes to ensure consistency and reliability. Main responsibilities include
  • Masters in chemical engineering, biomolecular engineering, or a related field
  • 5+ years of industrial experience with a proven track record of accomplishments, preferably in bio-industrial, or life sciences
  • Experienced in fermentation control system and software
14

Senior Associate Scientist, Immunology Resume Examples & Samples

  • Plan and execute scientific experiments
  • Analyze and interpret scientific data
  • Maintain primary and cancer cell lines and conduct routine cell culture tasks
  • Conduct various routine cell based assays to characterize drug compounds
  • Accurately maintain written reports and organize data
  • Trouble shoot
  • Role models for other scientists
  • Responsible for the completion of assignments that have an impact on functional goals
  • Bachelor’s degree in a scientific discipline with at least 8 years industry experience or Master’s degree with at least 6 years industry experience
  • Practical experience in, and a solid understanding of basic cell biology, immunology/immune-oncology, and assay development
  • Extensive experience with mammalian cell culture (primary cells and cell lines) using single cells and co-culture cell models. Experience using single compound treatment and combination treatment studies is essential. Prior experience with small molecules as well as biologics is preferred
  • Expertise with a variety of cell-based assay technologies including antibody-based detection methods (e.g. Western, ELISA, MSD, Luminex, immunoprecipitation), cell imaging (immunofluorescence, Incucyte, Cellomics), functional assays such as cell cycle and apoptosis and multiparameter flow cytometry is required
  • Excellent communication, presentation, collaboration and organizational skills are required as well as the ability to independently design, execute, and trouble-shoot experiments through completion
  • Data analysis skills and experience with a variety of scientific software applications are required
  • The successful candidate will be an ambitious self-starter, be motivated to apply his/her skills to meet diverse project needs, and enjoy working in a fast-paced dynamic team environment
  • Solid understanding of Immunology and relevant scientific principals
15

Senior Associate Scientist, Research Resume Examples & Samples

  • Facilitate establishment of contracts detailing specific assay, report and timeline requirements with CROs selected to perform bioanalytical sample testing
  • Serve as GBDD SMT representative and execute needed activities
  • Oversee operational aspects of bioanalytical and biomarker assay outsourcing required for preclinical and clinical studies with no direct supervision
  • Oversee testing of clinical and preclinical sample testing in routine and specialized clinical assays with no direct supervision
  • Coordinate input into clinical study documents such as the scope of work, CRFs and data and report delivery timelines
  • Coordinate the timing of sample testing as well as monitoring study activities at contract sites
  • Manage multiple studies across several programs and therapeutic areas
  • Manage outsourcing budgets, agreements and timelines as needed
  • Initiate bioanalytical development, transfer, validation and testing work orders
  • Interact with clinical data group on bioanalytical data deliverables
  • Oversee generation and completion of bioanalytical reports
  • Review bioanalytical reports and make recommendations for changes
  • Conduct technical audits of vendors as needed
  • Follow procedures according to established SOPs and other department guidelines
  • Will need to have understanding of both small and large molecule technologies
  • May write Standard Operating Procedures
  • May act as a qualified trainer for specific assays or procedures
  • May act as a technical subject matter expect at compliance audits
  • Other duties as assigned by supervisor
  • Good understanding of study activities
  • Ability to travel to CRO sites within and outside the USA when needed (very limited travel)
  • Excellent planning, organizational and communication skills
  • Work independently and as part of a team
  • Ability to maintain a healthy work/life balance in spite of work commitments. The role may necessitate working evening and/or weekend hours as necessary to meet project demands
  • Minimum 5 years previous industry experience in a laboratory ELISA, Flow Cytometry or PCR, LCMS assays or within specialty technology
  • Experience with project management and timeline management
  • Experience working with contract research organizations
16

Senior Associate Scientist Resume Examples & Samples

  • The Sr Associate Scientist will
  • Be responsible for the analytical support of process development projects in Small Molecule API development department
  • Minimum a Bachelor’s degree in Chemistry or related scientific field with at least 10 years experience in the field of analytical chemistry
  • Demonstrated capability to work with various IT systems
  • Experience with GMP regulations is preferred
  • Experience with other analytical techniques such as wet chemistry -titrations, specific optical rotation, UV spectroscopy, NMR
  • Technical knowledge and proficiency in ICP-OES and AAS
  • Good understanding of organic chemistry
  • Proven problem solving capacityR&D
17

Senior Associate Scientist Resume Examples & Samples

  • Routine maintenance and expansion of mammalian Human Embryonic Kidney cells and/or Chinese Hamster Ovary cells
  • Transient protein expression and cell harvesting
  • Affinity protein purification and protein characterization
  • Molecular biology and mutagenesis
  • Educational background: BS or MS (molecular or cellular biology, immunology, biochemistry, engineering, or related field)
  • At least 1 year of relevant experience in mammalian expression systems, molecular biology, and protein characterization
  • Training or experience in biological sciences focusing on protein expression, purification, protein engineering and characterization
  • Experience with mammalian expression systems, affinity chromatography, and wave bioreactors
  • Experience in protein biochemistry, including SDS PAGE protein gels, Western gels, ELISA, and analytical SEC
  • Experience with molecular biology and molecular cloning techniques including DNA isolation, PCR, and mutagenesis
  • Self-starter, able to prioritize work and work efficiently with minimal supervision and work across teams
  • Comfortable maintaining lab supplies and managing equipment autonomously
  • Excellent verbal/written communication, organizational and interpersonal skills
18

Senior Associate Scientist Resume Examples & Samples

  • Work with supervisor to design, execute and troubleshoot experiments and to analyze interpret results
  • Document and communicate experimental results clearly and concisely, may participate in writing manuscripts, scientific reports and patents
  • Continuously build personal understanding of scientific concepts underlying experiments, enabling development of effective and creative approaches to achieve company objectives
19

Senior Associate Scientist Resume Examples & Samples

  • B.A./B.S. with at least 9 years pharmaceutical research experience OR a M.S. with at least 6 years pharmaceutical research experience OR a PhD with relevant research experience is required
  • Experience in the immunology field is preferred
  • Previous experience setting up cell based assays (proliferation, ELISAs, transfections, siRNA/shRNA knockdown) is required; with stable clonal cell line generation is preferred
  • Experience isolating and characterizing immune cell populations from whole blood or tissues and setting up immuno-assays (i.e.: ADCC, cytokine release, T-cell biology or other functional assays) is preferredR&D
20

Senior Associate Scientist Resume Examples & Samples

  • Characterize novel enzymes, elucidate options for hit ID approaches, collaborate with screening scientists on direct binding studies, develop HTS assays, and perform mechanism-of-action studies on validated hits
  • Provide enzyme and inhibitor mechanistic data and insight and analyze biochemical and cellular SAR throughout different stages of the project
  • Collaborate in a highly multidisciplinary/matrix environment for the progression of drug discovery projects
  • BS in enzymology /biochemistry/biophysics/pharmacology with at least 10 years of experience OR a MS in enzymology /biochemistry/biophysics/pharmacology with at least 6 years of experience OR a PhD in enzymology /biochemistry/biophysics/pharmacology with relevant experience is required
  • Extensive experience and knowledge in majority of the following areas; mechanism-of-action studies, enzyme characterization, single turn-over kinetics and steady state kinetics are required
  • Strong background in enzymology, protein biochemistry, and assay development are preferred
  • Expertise in biophysics with extensive experience with SPR and ITC, mechanistic biochemistry and enzyme kinetics is preferredR&D
21

Senior Associate Scientist Resume Examples & Samples

  • Neuroinflammation/neurodegeneration background is highly preferable
  • General molecular biology skills (DNA/RNA isolation, qPCR), knowledge of IHC/IF
  • Experience with mammalian tissue culture techniques (primary cells and cell lines)
  • Significant experience with protein analysis (Western blot, ELISA, protein extraction)
  • Small rodent handling and dosing via standard delivery routes
  • Imaging and FACS analysis preferable
  • Strong commitment and high flexibility of work schedule is required
22

Senior Associate Scientist Resume Examples & Samples

  • L:I-RD2
  • Demonstrates keen knowledge of experimental design, underlying scientific principles, and possesses the ability to rigorously analyze and assess results and generate clear reports
  • Demonstrates independent scientific thinking, and is adept in problem-solving and adaptation of protocols
  • Experience with mammalian cell culture techniques, DNA & RNA isolation, PCR, and qRT-PCR
  • Knowledge of gene specific nuclease platforms, including TALENs, ZFN, CRISPR/Cas9, is highly useful
  • Experience with chromatin/epigenetic techniques such as ChIP-seq and genome-wide chromatin occupancy as well as experience with are preferred
  • Advanced skills in working with RNA, NGS library preparation, and experience with the Agilent Bioanalyzer instrumentation and DNA and RNA assays and analysis are a plus
  • Actively communicate with peer scientists to improve workflow, and identify and implement best methods for achieving group goals in a time-efficient manner
  • Work under guidance of a staff scientist
23

Senior Associate Scientist Resume Examples & Samples

  • Conduct routine cytokine profiling and immunophenotyping assays, analyze assay data, and report high quality results to support lead optimization efforts for ongoing drug discovery projects
  • Investigate, design, and develop assays to expand assay toolboxes and technologies for project advancement in collaboration with supervisor
  • Design, execute, and analyze PD experiments under the guidance
  • Enable and conduct medium throughput cytokine or immunophynotyping screening
  • Identify moderately complex obstacles to progress and troubleshoots using a limited set of resources
  • Perform as a role model supporting Celgene culture and follows policies; participates on cross-functional teams
  • Experience in cell culture, especially primary human cell culture
  • Expertise in the isolation, manipulation, and characterization of primary human T cells
  • Expertise in functional assays to characterize T cells such as cytokine production assays (ELISAs); cytotoxicity assays; and proliferation assays
  • Hands on experience in flow cytometry is required
  • Experienced with medium to high throughput cell based assay screening is preferred
  • Ability to analyze, interpret, and present data
  • Expert knowledge & demonstration of technical field
  • Generally independent in carrying out laboratory operations
  • Solid understanding of relevant scientific principals
  • Viewed as technically experienced and valued resource within department
  • Able to identify scientific and technical problems and potential solutions
  • Execute experiments independently
  • Interpret and discuss data
  • Familiar with literature
  • Communicate via meetings and reports
  • Able to coordinate CRO services
24

Senior Associate Scientist Analytical Devp Raw Materials Resume Examples & Samples

  • Execute analytical testing for APIs and raw materials in support of new sun care product development
  • Develop specifications for new APIs and raw materials
  • Manage reference standards and certifications
  • Work closely with other team members to install, qualify, daily use and maintenance of GIDC LIMS
  • Create specifications, protocols, reports and records, etc. in LIMS
  • Work on installation, qualification, calibration and maintenance of all instruments in the AD Lab
  • Create and update SOPs and/or Operation Instructions
  • Manage the data systems like Vision Publisher, Empower by coordinating the maintenance and work on resolving issues impacting the function of the systems
  • Accurately review scientific data to ensure compliance with all requirements
  • Bachelor’s degree in Chemistry or international equivalent with 4 or more years of proven experience
  • Master’s degree in Chemistry or international equivalent
  • Ph.D. in Chemistry with postdoctoral or international equivalent
  • Thorough knowledge of analytical instrumentation (HPLC, GC, AA, IR, UV-VIS) and wet chemical techniques with strong focus on HPLC
  • Positive "can-do" attitude and the ability to deliver results in a fast paced environment
  • Strong background in chemistry and good problem solving skills
25

Senior Associate Scientist Analytical Development Personal Care Resume Examples & Samples

  • Execute analytical testing procedures for early prototypes, informal stability, process optimization, clinical sample testing and cleaning validation sample testing required in support of new product development
  • Generating accurate scientific analytical data
  • Accurately interpret, document, and enter results into the LIMS database
  • Write analytical test methods, method development reports, method validation protocols, and method validation reports
  • Assist with troubleshooting analytical methods
  • Responsible for accurately reviewing scientific data to ensure compliance with all requirements
  • Bachelor’s degree in Chemistry or international equivalent with 4 or more years of experience
  • This individual must have a thorough knowledge of analytical instrumentation (HPLC, GC, AA, IR, UV-VIS) and wet chemical techniques with strong focus on HPLC
  • This individual must have a positive "can-do" attitude and the ability to deliver results in a fast paced environment
  • This individual must have an in depth working knowledge of various types of software including Word, Empower software, and Excel spreadsheets
  • This individual must have a strong background in chemistry and good problem solving skills
  • Communicate and collaborate effectively with other scientists within the group and across sites
26

Senior Associate Scientist Resume Examples & Samples

  • Execute formulation development activities such as performing hands on execution of experiments in laboratory prototyping, material characterization (i.e. product and ingredients), accelerated stability studies to screen prototypes, quality by design and design of experiments execution, initial process design drafting, and formulation development reports
  • Help execute Formulation Development strategy for assigned projects
  • Clearly identify and escalate formulation issues to supervisor and project team
  • Test potential formulations by working with cross-functional project teams to determine experimental and stability test requirements and reviewing with cross-functional project team on data and conclusions for product testing and stability
  • Laboratory support activities such as formulation equipment “owner” as a subject matter expert, raw material ordering and naming, and ensuring equipment is in working order
  • Participate in Innovation activities by making prototypes for proposed ideas and concepts, proactively suggest new product ideas based on consumer needs or innovation strategy, and a actively look for external technologies and capabilities to apply for internal prototypes (if applicable)
  • Bachelor of Science in Pharmaceutical Sciences/Chemical Engineering/Chemistry
  • At least four (4) years of experience in Formulation or Processing Development
  • Experience working on OTC/pharmaceutical drug/cosmetic/nutritional products or development with various product form development, processing and unit operations
  • Passionate about innovation, research, hands-on laboratory work and learning new skills
  • Demonstrated experience working in diverse and cross-functional teams
  • Excellent written and verbal communication in English
  • Experience and understanding of cGMP requirements
  • Demonstrated behaviors of trust, collaboration, experimentation and customer focus
27

Senior Associate Scientist Analytical Development Resume Examples & Samples

  • Develop and evaluate analytical methods and also provide analytical support for new product development
  • Design, execute and interpret complex laboratory experiments in a fast-paced environment
  • Generate accurate scientific analytical data
  • Accurately interpret, document and enter results into the LIMS database
  • Write analytical test methods, method development reports, method validation protocols, method validation reports
  • Compile accurate scientific data in various reports, or other documents
  • In depth working knowledge of various types of software including Word, Empower software, and Excel spreadsheets
  • Effective communication and collaboration with other scientists within the group and across sites
28

Senior Associate Scientist Resume Examples & Samples

  • Initiates an perform laboratory testing and record data according to GxPs, SOPs, and Protocols
  • Author and revise SOPs and Protocols
  • Perform GXP laboratory related investigations
  • Correct issues that may not be immediately evident, using existing or new processes
  • Provide training to scientific staff
  • Contribute to database development and suggest improvements to systems
  • Lead method co-validations and method transfers
  • Lead and serve as representative on cross-functional teams
  • B.S. or equivalent in Chemistry, Biochemistry or related discipline is required with at least 8 years of related laboratory experience OR a M.S. with at least 5 years of related laboratory experience is required
  • Experience in analytical, QC or relative industry labs with solid understanding of large molecule testing is required
  • Experience in one or more of the following: SE-HPLC, cSDS, cIEF, or ELISA techniques is required
  • Knowledge of cGMP regulations, basic understanding of data trending and use of electronic notebook and Empower is preferred
  • Excellent communication skills (written and oral) and the ability to work in a cross functional environment are required
  • Technical writing experience (SOPs and Protocols) is required
  • Previous project leadership experience is required
29

Senior Associate Scientist Resume Examples & Samples

  • Actively participate in the development of immune cell assays for drug candidate evaluation, mechanistic studies, and biomarker development
  • Evaluate innovative technologies for developing biomarker assays
  • Assist in the coordination of external collaborations contract research laboratories
  • Perform cell biology, molecular biology, and biochemical techniques including primary and tumor cell culture, lymphocyte activation and cytotoxicity assays, multi-parameter flow cytometry, ELISA, ELISpot, RT-PCR, RNA preparation, viral transduction, mammalian cell transfection, immunoprecipitation, and western blotting
  • Perform a wide range of assigned research experiments with efficiency, accuracy and attention to detail, conduct analysis and report results
  • Independently follow protocols and function with minimal supervision
  • Contribute to design of experimental procedures and search literature for targeted information
  • B.S. with 8 years or or M.S. with 6 years experience as a research associate and at bench in an industrial setting
  • Solid understanding of scientific mechanisms and experimental techniques, with knowledge of immunology and cancer cell biology preferable
  • Experience working with and coordinating CROs
  • Familiarity with techniques related to biomarker research and development
  • Familiarity with and experience in the drug development process from discovery through IND filing in an industry setting
  • Ability to multitask, independently organize time and plan specifics of work
30

Senior Associate Scientist Resume Examples & Samples

  • Mass spectrometry (LC/MS, GC/MS, ICP/MS)
  • FTIR, NIR, Particle size testing; ICP/OES, DSC, CD, intrinsic fluorescence
  • BS degree with 1-3 years relevant experience
  • Knowledge/Skills Requirements: Electrophoresis, mass spectrometry, FTIR, NIR, metal testing
  • Ability to mentor/train peers as necessary
  • Members of staff within LMAC
31

Senior Associate Scientist Resume Examples & Samples

  • Be a key member of a team that will support IPD’s metabolic engineering and strain development platforms encompassing a broad array of microbial hosts, in particular, but not necessarily limited to gram negative/positive bacteria and yeast
  • Take an active role in designing experiments and testing hypotheses in collaboration with multiple team members and teams within the division
  • Execute high throughput DNA and strain construction in a timely manner with high fidelity
  • Shepherd microbial strains to the screening group and take an active role in data analysis
  • Work in partnership with other IPD teams (fermentation, assay development and screening, analytical) to advance projects
  • Tracking and resolving technical challenges
  • Suggest and implement process improvements
  • Maintain timely documentation of laboratory work
  • Evaluate data and make scientific presentations
  • Maintain knowledge of current bio-industrial/metabolic engineering literature
  • BS in genetics, molecular biology, microbiology, biochemistry, chemical engineering or a related field
  • Three (3) + years of relevant industry experience or MS with relevant research experience
  • A proven track record of accomplishments and timely delivery on goals
  • Experience in at least one of the following
  • Maintain a high degree of accuracy and attention to detail while working in high throughput
  • Build and maintain positive relationships with coworkers and managers
  • Energized by accomplishments, overcoming challenges and excellence in the workplace
32

Senior Associate Scientist / Scientist Resume Examples & Samples

  • Perform analytical activities for small molecule drug substances and drug products according to regulatory requirements for investigational products
  • Develop and transfer in-house developed analytical methods to external contract organizations
  • Manage analytical activities at external contract organizations and provide support during the manufacturing campaigns for drug substances and drug products
  • Provide analytical support for internal Process Chemistry and Formulation functions
  • Maintain proper documentation of laboratory experiments
  • Author internal analytical reports in support of regulatory filings and review analytical documents and data generated by external contract organizations
  • Participate in technical visits and audits to external contract organizations
  • M.S. or Ph.D. in Pharmaceutical Sciences, Chemistry, or related fields with a minimum 3 years of hands-on experience in performing analytical development and testing activities in the pharmaceutical industry
  • Experience with analytical method development and validation for small molecule drug substances (NCEs) and drug products is a must
  • Strong proficiency with UPLC, HPLC, GC, Dissolution, and solid state characterization (e.g. DSC, TGA, XRPD) instrumentation
  • Knowledge of the CMC regulatory requirements (e.g. FDA, EMEA, and ICH) and thorough understanding of working in a cGMP environment is highly desirable
  • Strong technical, project management, and interpersonal skills
  • Ability to work independently using critical and creative thinking skills to solve problems and advance the development objectives of the company
  • May require up to 15% travelling
33

Senior Associate Scientist Resume Examples & Samples

  • Develop in vitro assays, ex vivo cell-based models, and technology platforms to evaluate PK/PD relationship, efficacy and mechanism of action of therapeutic drug candidates
  • Develop PK and immunogenicity assays for protein and antisense oligonucleotide drug candidates
  • Establish technical excellence in biomarker and bioanalytical assay development serving as a departmental subject matter expert
  • Recognize and actively troubleshoot data anomalies to ensure high quality of final data
  • Interact with various project teams as a liaison to update project progress and share technical insights
  • Expertise in ligand binding and cell-based assays, utilizing a variety of technology platforms
  • Hands on experience in the development and validation of biomarker and/or bioanalytical assays in the preclinical and clinical setting considered a plus
  • Excellent assay troubleshooting skills and the ability to identify and validate cutting edge assay technologies
  • Must demonstrate a thorough knowledge of experimental design, underlying scientific principles, and the ability to independently interpret results
  • Relevant experience in immunology/neuroimmunology, bioanalytical sciences, and/or development of immunomodulatory therapies
  • Experience in standard molecular biology and protein biochemistry techniques (e.g. real-time PCR, DNA cloning, protein purification, Western blotting, immunoprecipitation, and enzymatic assays) is required
  • Demonstrated track record of working independently or with minimal supervision in managing multiple projects and priorities
34

Senior Associate Scientist Resume Examples & Samples

  • Core member of a dynamic, scientifically driven team dedicated to the discovery and development of elegant chemical syntheses and processes for active pharmaceutical compounds
  • Develop scalable chemical manufacturing processes by planning, designing, executing, interpreting, and clearly documenting experiments
  • Assist with the manufacture of development candidates for pre-IND and clinical studies
  • Assist with technology transfers to and manufacturing of GMP Drug Substance at Contract Research Organizations
  • Currency with required GMP training and qualifications
  • Prepare technical reports and oral presentations
  • M.S. +5 years, or B.S. +8 years in Chemistry or Related Field
  • Strong organic laboratory skills and knowledge of organic synthesis
  • Proficiency in the use of NMR, MS, IR, HPLC, and GC. Experience with process automation platforms, DSC, TGA, and/or XRD are a plus
  • Ability and drive to learn and implement relevant principles of chemical engineering, material science, analytical chemistry, and regulatory guidelines
  • Strong interpersonal skills and the ability to work in a fast paced, multidisciplinary, matrixed environment
  • Ability to work independently or in a team under deadline. Strong verbal and written communication skills are essential
  • Kilo lab or pilot plant experience is desired
  • Familiarity with GMP/GLP practices and standards are a plus
35

Senior Associate Scientist Resume Examples & Samples

  • Troubleshoot and/or optimize analytical methods for clinical and commercial programs
  • Write, review, and sign off on technical protocols and reports. Author and review subsequent regulatory filings
  • Provide technical support for analytical method validation and transfer during regulatory inspections
  • Travel internationally as needed
  • LI-CTL2
  • Technical expertise in bioassays and potency testing for biologics (e.g. FRET, ALPHA-Screen, DELFIA binding assays, proliferation assays, ELISAs, cell-based assays)
  • Experience with utilizing Softmax Pro and Parallel Line Analysis (PLA) software for bioassay data analysis
  • Experience with automation of bioassays highly desirable
  • Relevant experience in analytical method development and validation
  • Statistical experimental design and data analysis with JMP software
  • Experience training and mentoring others
36

Senior Associate Scientist Resume Examples & Samples

  • A Bachelor’s degree in Science or Engineering is required
  • At least four (4) years of experience in Technical Services and/or Validations within a Pharmaceutical, Medical Devices or Consumer Products industry is required
  • Previous experience working with solid dosage processes and technologies is required
  • Knowledge in Process Analytical Technology (PAT), data base and modeling is highly preferred
  • Strong knowledge of scientific investigation processes and statistical analysis/tools is required
  • Experience in validation and qualification, troubleshooting, and technical writing is required. Experience in project management would be an asset
  • Knowledge of documentation Systems (Docspace, Trackswise, eLab), Inventory control Systems (SAP) and Learning Management Systems (ComplianceWire) is preferred
  • Must be proficient in Microsoft Office programs (PowerPoint, Word, Excel, Outlook). MS Project and Minitab are highly preferred
  • Must be fully bilingual (English and Spanish, oral and written)
  • This position requires up to fifteen percent (15%) of domestic and international travel.R&D
37

Senior Associate Scientist Resume Examples & Samples

  • B.S. in biochemistry or biophysics, or related field with at least 9 years of pharmaceutical industry experience or B.S. and M.S. in biochemistry or biophysics, or related field with at least 6 years of pharmaceutical industry experience
  • Industry experience with the characterization of small-molecule interactions with proteins is required
  • Expertise with biophysical methods such as SPR, thermophoresis, ITC and mass spectrometry is required
  • Experience working with and guiding external collaborators in industry or academia is desired.R&D
38

Senior Associate Scientist Cheminformatics Resume Examples & Samples

  • Actively participate in Amgen Asia R&D projects by providing expertise in molecular modeling, cheminformatics and computer-aided drug design
  • Establish, maintain and apply state-of-the-art cheminformatics tools and technologies to the drug discovery projects
  • Scientific network within cheminformatics and related areas with stakeholders to ensure good alignment
  • Build external visibility and maintain good publication record
39

Senior Associate Scientist Resume Examples & Samples

  • Molecular biology and mutagenesis including subcloning, site-directed mutagenesis, PCR and DNA manipulation
  • Protein and antibody in silico design
  • Protein expression & isolation
  • Protein characterization including SDS-PAGE protein gels, Westerns, analytical SEC, ELISAs, SPR
  • Affinity maturation & antibody optimization (phage, yeast, mammalian, or mRNA display; rational design techniques)
  • Training or experience in biological sciences focusing on protein engineering, molecular biology, protein expression, purification, and characterization
  • Experience with molecular biology and molecular cloning techniques including DNA and RNA isolation, PCR, and mutagenesis
  • Experience with bacterial and mammalian expression systems, affinity chromatography, and protein quantification
  • Some experience generating or working with DNA libraries for display or next-generation sequencing is desired
  • Computer skills required: Microsoft Word, Excel, Outlook, BLAST, Vector NTI or equivalent
40

Senior Associate / Scientist Resume Examples & Samples

  • Ph.D. in Materials Science and Engineering, Corrosion or Electrochemistry
  • Ability to work within project teams with a strong desire to contribute
  • Specialized knowledge of corrosion science with a strong background in electrochemical techniques is required
  • Knowledge of failure analysis and coating technology is desired
41

Senior Associate Scientist Ba Chemist Resume Examples & Samples

  • Master degree with minimum of 1 year of relevant experience is required
  • Degree in Chemistry or a related field such as Biochemistry, Biology, or Pharmaceutical Sciences, with training in Bioanalytical techniques is preferred
  • Working knowledge and functional experience with using modern LC/MS instrumentation (Thermo Fisher Orbitrap and Sciex Triple Quad preferred) in conjunction with various sample prep techniques (i.e. oligonucleotide extraction, protein precipitation, SPE, chemical derivatization) are required
  • Excellent interpersonal, organizational, and oral/written communication skills with the ability to thrive in a goal driven team environment are preferred.Pharmacokinetics
42

Senior / Associate Scientist Resume Examples & Samples

  • BS, with experience working on in vitro assays in CV/CNS,
  • Design and interpretation of in vitro experiments utilizing mammalian cell lines and/or primary cells. Mammalian cell culture and handling, along with screening technologies utilizing imaging and electrophysiology
  • Proficiency in laboratory instrumentation and data collection tools. Experience of the application of statistical approaches to the analysis of in vitro data
  • Degree focused in pharmacology, physiology, neuroscience or a related biological discipline, with industrial experience
  • Experience with automation, screening, plate-based assays and statistical analysis
43

Senior Associate Scientist Resume Examples & Samples

  • Integration, analysis and interpretation of high dimensional data generated from preclinical and clinical compound profiling studies and disease models. The transition to tractable molecular determinants and models will demand close coordination with the experimental scientists to identify relevant and testable hypotheses and assayable readout combinations
  • Collaborations with Therapeutic Area/Disease Area Stronghold scientific will provide an opportunity to design and implement a choice of optimal analysis and modeling approaches, also driven by incentives to publish the non-proprietary new science
  • Contribution to the design and the selection of new experiments, optimal experimental design and hypothesis driven studies is an integral part of the role
  • Experience in analysis and modeling of control mechanisms of heterogeneous multicellular processes is preferred
  • Experience in handling high-dimensional single cell data, e.g. mass cytometry, high-content imaging derived features is required
  • Excellent communication, reporting and team working skills, yet able to work independently is required.Clinical Data Management
44

Senior Associate Scientist Resume Examples & Samples

  • Execution of ASO formulation and process development study protocols, stability and product characterization studies
  • Conducting bench scale studies to develop ASO drug delivery systems
  • Supporting ASO fill-finish process development work at manufacturing sites for parenteral drug formulations and delivery systems
  • Performing analytical characterization of study samples using various biochemical or biophysical methods
  • Closely interfacing with chemical synthesis, purification and analytic groups to support ASO manufacturing platforms
  • Presenting scientific data to technical teams, ability to manage several projects simultaneously, and excellent communication skills, both written and oral
  • Sound knowledge of formulation development and stabilization of therapeutics, preferably with hands-on experience with oligonucleotides
  • Understanding of drug product manufacturing process operations such as mixing, sterile filtration, extractable/leachable assessments and container filling/closing
  • Experience in developing and analyzing drug delivery systems such as microspheres and liposomes
  • Experience in analytical and characterization methods such as chromatography, spectroscopy, calorimetry and particle analysis technologies
  • Use of membrane technologies for preparing formulations, experience with aseptic technique for stability and preclinical material preparation
45

Senior Associate Scientist Resume Examples & Samples

  • Demonstrate the ability to design, perform, interpret, troubleshoot and report complex data
  • BS with at least 10 years of experience OR a MS with at least 6 years of experience is required
  • Experience in the cancer field is required
  • Translational Research experience in a biotech or pharmaceutical environment is required
  • Cell/molecular biology skills are required - Transfections, IHC staining and imaging of TMAs and whole tissue sections, western blotting, siRNA/shRNA, qRT-PCR (including using Fluidigm Biomark platform), immunofluorescence, FACS and ELISA, next generation sequencing
  • Experience performing drug sensitivity assays is requiredR&D
46

Senior Associate Scientist, Immunology Resume Examples & Samples

  • Design, plan, and execute cell based assays and troubleshoot existing protocols with guidance
  • Perform high quality and well controlled immunological assays with human and animal primary immune cells including cell stimulation, cytokine analysis,, and flow cytometry with minimal supervision
  • Support scientists in execution of proof-of-concept studies. Generate and independently analyze multi-parameters data sets using appropriate analytic programs
  • Maintain well written and accurate research electronic notebook detailing work undertaken
  • Extensive experience in isolation, culture, and characterization of primary immune cells from human and animal tissues
  • Strong hands-on experience with common immunological assays (cell activation, proliferation assays, cytokine analysis by FACS and ELISA, and multiplex assays)
  • Experience with lymphocyte and myeloid cell activation and characterization assays, multi-parameter flow cytometry, ELISA, ELISpot, RT-PCR, RNA preparation, viral transduction, mammalian cell transfection, immunoprecipitation, and western blotting
  • Team player, detail oriented and organized
47

Senior Associate Scientist Resume Examples & Samples

  • Responsible for supporting and further developing the center of excellence (CoE) for analytical assay development and supporting two parenteral pilot plants in a GMP regulated set-up
  • Understanding the process and urgency of providing analytical support to local and global customers
  • Subject matter expert in the CoE for assay development according to international guidelines (e.g. ICH)
  • Excellent German communication skills; Good command of English is a plus
  • Write scientifically sound and concise reports in English
  • B.S. or M.S. with experience in life science, analytical or pharmaceutical sciences
  • Experienced in analytical development or material science with significant emphasis on fluorescence microplate assays in a pharmaceutical or other GMP regulated industry
  • Self-starter and problem solver with determination to achieve common goals
  • A real teamplayer with scientific curiosity and willingness to “go the extra mile”
  • Demonstrated ability to influence at all levels, to positively impact productivity and business results
48

Senior Associate Scientist Resume Examples & Samples

  • Serve as analytical technical expert to support the introduction of both early as well as late phase clinical products to the API Leiden pilot plant or JSC facility respectively
  • Participate in and/or have an analytical lead role in new product introduction projects
  • Participates in life cycle management teams to identify, develop and implement analytical improvements
  • Serve as the analytical technical expert during development, investigations and regulatory inspections
  • Designs experiments, writes protocols, serves as study director during execution and evaluates end results for scientifically supported conclusions and recommendations that are documented in appropriate technical reports
  • As a member of the Analytical team, the candidate is expected to: Create an environment that values innovation, leadership, scientific excellence, urgency and personal accountability
  • Analyzes data and highly complex situations involving the evaluation of tangible and identifiable variables to arrive at creative and effective solutions
  • Focuses on continuous improvement in the development of new or refined methods, processes, and/or scientific procedures
  • Interacts on a regular basis with counterparts in the analytical organization to become aware of potential issues regarding performance and to maintain well developed lines of communication between organizations
  • Self-reliant, able to work within and/or lead project teams, providing leadership, flexibility and positive attitude
  • MSc or PhD in Biochemistry, Bioprocess technology or similar relevant topic
  • Preferably 2 to 3 years relevant experience in a biopharmaceutical/biotechnological environment
  • Preferably experience with characterization of biopharmaceutical products
  • Analytical and innovative thinker
  • Excellent communication skills, both oral and written, preferably fluent in both Dutch and English, to support working in an international environment with frequent contact in the United States, Ireland and Belgium as well as in Leiden
  • Highly results driven, with focus on customer satisfaction and on-time completion of projects
  • Adaptable and flexible
  • Open to accept practical as well as theoretical assignments
49

Senior Associate Scientist Resume Examples & Samples

  • Maintaining qualification and re-qualification schedules for RM and CR, and work with QC sites to obtain the data necessary to prepare qualification and requalification documents and issue Certificate of Analysis
  • Work with QC sites and statisticians to compile trending data as appropriate for large molecule reference materials and critical reagents
  • Write SOPs, Specifications and Protocols to support all projects and programs
  • Prepare the appropriate sections for regulatory filings and support inspections and audits
  • BS with at least 5 years experience OR MS with at least 3 years experience in Chemistry, Biochemistry or related discipline is required
  • Solid understanding of release and stability testing of large molecules is required
  • Large Molecule experience with any of the following: HPLC, ELISA, Bioassay, Capillary Electrophoresis, Characterization and cIEF is preferred
  • Knowledge of cGMP regulations, basic understanding of data trending and experience with process excellence methodology is preferred
  • Excellent communication skills (written, oral and presentation) and the ability to work in a cross functional environment are required
  • Strong technical writing experience (SOPs, Protocols, and Qualification Reports) is required
  • Regulatory writing experience (INDs, NDAs, BLAs) is preferredR&D
50

Senior Associate Scientist Resume Examples & Samples

  • Leading and participating in the design of experiments, executing the planned experiments, and optimizing purification process steps, and data analysis for early and late stage projects
  • Lead design and execution of the development studies to identify and determine process parameter ranges for purification process steps
  • Provide technical leadership to others and make decisions to set directon for the project
  • Record and analyze experimental data, verify data integrity and accuracy, and report/summarize findings to the project team, and also write technical documents
  • Work in a team environment as well as contributing individually to meet project timeline and objectives
  • An MS in Chemical Engineering or Biological Sciences or Biochemistry and with at least 3 years of relevant experience OR a BS in Chemical Engineering or Biological Sciences or Biochemistry and with at least 5 years of relevant experience is required
  • Previous experience in scale-up and transfer of a purification process to clinical and commercial GMP manufacturing is required
  • Familiarity with process development of viral based products is preferred
  • Familiarity with and hands-on experience with analytical methods typically used in the manufacture and characterization of recombinant proteins is preferred
51

Senior Associate Scientist, Protein Lab Resume Examples & Samples

  • A minimum of a BA/BS combined with 9 years’ experience in a Biological/Chemical discipline is required
  • A MA/MS with 6 years of experience in a Biological/Chemistry discipline is preferred, but not required
  • The successful candidate should have experience using antibody techniques for measuring and studying proteins in biological samples
  • Experience using computer based data acquisition and analysis is preferred
  • The ability to learn new instrumentation for assay development is required
  • The position is located in La Jolla, CA and may require < 10% travel.Biology
52

Senior Associate Scientist Resume Examples & Samples

  • Guide pharmaceutical development teams on the selection of materials based on scientific, quality and regulatory criteria
  • Collaborate with raw material suppliers and internal partners to establish effective raw materials control strategies based on understanding and importance of raw material in API and DP supporting Janssen manufacturing and CMOs
  • Develop raw material specifications, e.g., cell culture media, chromatography resins, excipients and adjuvants
  • Support technology transfer and life cycle management of materials used in the clinical and commercial supply chain including technical assessment of supplier-initiated and CMO-initiated changes
  • Review and implement industry and regulatory requirements for raw materials, e.g., ICH guidance
  • Support enhanced characterization and data analysis, e.g., latent variable statistical models
  • Support for supplier audits/selection as required
  • Identify and coordinate analytical characterization with the internal and external labs and perform testing as applicable
  • Actively participate on cross-functional R&D and manufacturing teams to advance projects goals and deliverables related to raw materials
  • Participate in project and scientific meetings to share information, knowledge, ideas, and judgment to help establish valid scientific directions in product development or investigations
  • Ensure compliance with safety, GMP, quality and scientific principles
  • A Bachelors in Chemistry, Biology, Materials Science and Engineering, Biochemical Engineering, Chemical Engineering, Pharmacy/Pharmaceutics or a related field with at least 9 years of experience OR a Masters in Chemistry, Biology, Materials Science and Engineering, Biochemical Engineering, Chemical Engineering, Pharmacy/Pharmaceutics or a related field with at least 6 years of experience is required
  • Demonstrated proficiency in characterization of cell culture media including cell culture performance evaluation using stationary, shake flask, automated cell culture systems, and/or bioreactors is required
  • Demonstrated proficiency in the analytical characterization of cell culture media is required
  • Demonstrated proficiency in qualification of cell culture media and analytical characterization of cell culture media is strongly preferred
  • Demonstrated competency and experience in product development within the pharmaceutical industry is preferred
  • Demonstrated competency and experience in use of project management tools (e.g., MS Project), spreadsheet and databases are preferred
  • Demonstrated experience is lean and/or six sigma methodologies and tools is preferredR&D
53

Senior Associate Scientist Resume Examples & Samples

  • Perform analytical methods necessary for the characterization and release of active biological ingredients and vaccine product
  • Documentate and communicate results in electronic laboratory notebooks, technical reports, oral/visual presentations
  • Have a basic understanding and utilize the statistical methods employed in immunoassays
  • Partner with statistics group to design experiments and report data
  • BS/MS in immunology, virology, biochemistry, veterinary sciences or animal science or other related discipline, at least 2-4 years industry experience preferably in the vaccine industry
  • Good oral and written communication skills
  • Academic or industry experience in a laboratory setting, specifically in bacterial or viral characterization
  • Skills and past experience in experimental design, technical problem solving and continuous improvement
54

Senior Associate Scientist Resume Examples & Samples

  • Designing and optimizing various formulation and filling unit operations including freeze/thaw, mixing, sterile filtration, vial and syringe filling and lyophilization, and overseeing the execution of pilot to commercial scale fill/finish manufacturing process
  • Perform stability studies, using biochemical and biophysical properties, on experimental and target formulations; and will perform studies to evaluate the chemical and physical compatibility of formulations with container/closure components, manufacturing and administration equipment
  • Perform technical analysis of the project data including trending of data
  • Author technical reports and be involved with presentations of the data
  • Follow general laboratory safety procedures, as related to biologically derived materials
  • Collaborate with contacts inside the company including scientific staff as well as scientists in related functional areas such as Research, Process Sciences, Devices, QC/QA, Clinical, Manufacturing, Toxicology, Regulatory (CMC)
  • B.S. in an appropriate scientific discipline with at least 6 years of related laboratory experience OR a MS with at least 4 years laboratory experience OR a PhD with relevant experience is required
  • Demonstrated working knowledge in formulation and fill/finish process development for therapeutic products is preferred
  • Working knowledge of numerous biochemical, biophysical and analytical methodologies such as HPLC, CD, fluorescence and UV spectroscopy, cIEF and cSDS, particle analyzers, etc. is required
  • Experience with aseptic process validation, scale up and technology transfer of liquid and solid dosage forms including lyophilization is preferred
  • Familiar with pharmacy procedures for drug preparation and human administration is preferred
  • Working knowledge of GLP or GMP requirements is preferred3592170302
55

Senior Associate Scientist Resume Examples & Samples

  • Design and conduct in vivo toxicology studies. Candidate should be proficient in test article administration by oral and parenteral routes, performing clinical observations, blood collection and necropsy
  • Perform clinical chemistry and hematology sample analyses
  • Provide comprehensive study data analysis and reporting
  • Communicate study findings and outcome to toxicology management
  • Serve as study director for in vivo exploratory toxicology studies with oversight of all aspects of study conduct, including protocol generation, in-life activities, data summary and interpretation, and study report preparation
  • Opportunity to monitor non-GLP toxicology studies conducted at contract research organizations
  • Support operational activities such as managing study inventory and scheduling, ordering compounds, histology specimen management, and quality control/data assurance of data and deliverables
  • Serve as an independent contributor to developing and implementing new methods and technologies, including flow cytometry applications
  • Experience with the design and conduct of in vivo toxicology/pharmacology studies
  • Familiarity with electronic data capture systems
  • Contributes individually as well as on cross functional teams
  • Familiarity and ease of use with GraphPad Prism, Microsoft Word, Excel, PowerPoint and Outlook
  • Occasional weekend and evening hours required
56

Senior Associate Scientist Resume Examples & Samples

  • Master’s degree and 3 years of scientific experience
  • 2+ years of protein therapeutics drug discovery and development experience in biotech industry, basic understanding of protein therapeutics DMPK
  • Strong knowledge in cell biology or immunology or oncology and will apply their biology/protein biochemistry expertise to independently design and execute studies to answer key project related DMPK questions
  • Demonstrated proficiencies with multi-color flow cytometry analysis and knowledge/expertise in protein biochemistry
57

Senior Associate Scientist Clinical Biomarkers Resume Examples & Samples

  • Master’s degree & 3 years of scientific experience
  • Masters in pharmaceutical, chemical, or biological science
  • 2 years’ experience developing and running clinical-grade assays, preferably with experience with multiple assay formats
  • Experience in assay development and qualification and analysis of clinical samples
58

Senior Associate Scientist Resume Examples & Samples

  • Conduct biochemical and cell-based experiments/assays to evaluate novel mechanisms and interrogate the biology of new therapeutic targets for AD
  • Critically analyze and interpret data, and meet delivery deadlines
  • Work closely with and communicate results to multi-disciplinary and cross-functional teams
  • Master’s Degree in Neuroscience
  • 3+ years of experience in neuroscience and neurodegenerative diseases
  • Experience/expertise in culturing primary neurons, iPSC-derived neurons and immortalized cell lines
  • Experience with CRISPR and iPSC technology
  • Experience developing a wide range of cell-based assays, and in interrogating a variety of cellular signaling pathways
  • A high degree of computer literacy and excellent analytical/problem-solving skills
  • Good organizational skills with the ability to independently design and execute experiments, and interpret results
  • Outstanding interpersonal and communication skills, and superior multi-tasking abilities
  • Highly motivated and adaptable individual who enjoys working in a team environment and welcomes new challenges
59

Senior Associate Scientist Resume Examples & Samples

  • Master’s degree and 4 years of Scientific experience
  • 4+ years of focus or specialization in synthetic organic or medicinal chemistry (academic and/or industrial)
  • Demonstrated ability to scout and troubleshoot synthetic routes, and perform high difficulty synthetic chemistry
  • Clear understanding of structural determination using NMR and Mass Spectral techniques as well as knowledge of purification methods
  • Demonstration of good lab practices, with particular attention to safety
  • Excellent communication skills (both written and oral), leadership skills and the ability to work well in teams
60

Senior Associate Scientist Resume Examples & Samples

  • 1) Driving wet lab efforts with a focus on establishing and utilizing a variety of cell based models (including iPSC, primary cell, organoid and three-dimensional) to develop assays to predict and investigate drug safety issues
  • 2) Application of an array of cell and molecular biology techniques to derive insight into molecular pathways that are perturbed by potential therapeutics or target intervention including a variety of ‘omics approaches
  • 3) Function as senior bench scientist in group providing mentorship and training for other associates within the team
  • 4) Interface with other teams and groups with within Amgen and the external community to establish robust experimental platforms and techniques to further our research goals
  • 5) Analysis, interpretation, meticulous documentation and presentation of data in group, department and project team meetings
  • 6) Assessment and development of new technologies and approaches that drive efficiency and/or allow us to address key questions around drug safety in humans
  • Masters degree in molecular biology, cellular biology or related discipline with 7+ years of experience in cellular, biochemical, or genomic research within the biotechnology industry
  • Significant experience in a variety of cellular, and molecular biology/toxicology approaches and techniques. Experience in three-dimensional tissue models and organoids is strongly preferred
  • Expertise in the establishment of high throughput cell based assays with a particular focus on phenotypic readouts
  • Comfort in working in a highly interactive and vibrant environment designed to promote frequent interaction and brainstorming
61

Senior Associate Scientist Resume Examples & Samples

  • Generating and communicating in vitro assay data to support the progression of Cardiometabolic Disorders research team
  • Timely record keeping and data analysis
  • Operating and maintaining laboratory equipment
  • Develop and validate in vitro target-based assays including binding assay and enzyme kinetic assays
  • Knowledge of assay development in drug discovery setting
  • Familiar with technology used in assay development, including microplate readers and automated liquid handling systems
  • Experience in protein overexpression and purification
  • Knowledge of technologies commonly used in HTS and cardio-metabolic diseases will be preferred
  • Excellent problem-solving skills and ability to multi-task
  • Excellent communication skills, the ability to work in team-oriented environment and strong interpersonal skills
  • Ability to use a variety of computer software including Graphpad Prism, Excel, Powerpoint and Word
62

Senior Associate Scientist / Scientist Resume Examples & Samples

  • Bachelors with 3-5 years of experience or Masters with 1-3 years of experience in a biological science area, veterinary or livestock industry or research experience in an academic institution or the pharmaceutical industry
  • Excellent organizational, decision-making and interpersonal skills as well as outstanding written and oral English communication skills
  • Self-motivated with high quality standards (communication, documentation) and attention to detail
  • Familiar with and comfortable with appropriate computer programs (MS Word, EXCEL, PowerPoint, and MS Outlook)
  • In depth knowledge of various global regulatory authorities, including FDA-CVM, VICH Guidelines, and GLPs governing the conduct of preclinical safety studies
  • Ability to understand, interpret and explain study designs and outcomes to others
  • Experience with managing and troubleshooting large toxicology programs at CROs, for various species
  • Experience in multisite GLP studies
63

Senior Associate Scientist Resume Examples & Samples

  • Solid scientific background in translational/biomarker research is required. Proactive participation and contribution to scientific community within JNJ will be expected
  • The successful candidate is expected to establish and manage technical platforms, such as IHC, to support biomarker research
  • The successful candidate will be expected to work efficiently in a multi-task environment, and to supervise junior scientists to deliver hands-on work according to priorities and timelines
  • The candidate should have a MD or PhD in biology, molecular biology, pathology, biochemistry or a related field, with minimum five years of industry experience in pre-clinical drug discovery or translational research, preferably in a pharmaceutical setting or other relevant healthcare industry
  • Hands on experience with cutting edge cellular and molecular technologies related to Oncology biomarker research would be required
  • Experience of managing biomarker platforms such as IHC would be highly desired
  • Experience working with global and regional partners (internal and external) is highly preferred
  • Demonstrated ability to work in a team oriented environment
  • Good written and oral communication skill in both English and Chinese1700156109W
64

Senior Associate Scientist Resume Examples & Samples

  • Assay development, writing protocols, reports, and performing and coordinating testing to support analytical development, manufacturing process development, process validations, and manufacturing investigations across functional groups
  • Accurate capture of data in a timely manner, including maintenance of detailed records in compliance with applicable cGMP, safety, and environmental requirements is expected and the successful candidate will ensure data integrity and protocol compliance
  • Providing technical support with development and QC laboratories is expected and the successful candidate will also support Quality Assurance, Regulatory Affairs and Process Development groups for all phases of product development as well as ongoing support of analytical methods for marketed products
  • Bachelor's degree in Biology, Chemistry, Pharmacology or other relevant scientific field, with at least 4 years of industry experience OR a Master's degree with at least 2 years of industry experience or with relevant academic experience is required
  • Experience in performing bioassays, binding assays and/or immunochemical techniques, including flow cytometry and immunoassays is required
  • Experience with surface plasmon resonance is preferred
  • Experience with therapeutic proteins, including antibodies, cell and gene therapy and/or vaccines is preferred6756170330
65

Senior Associate Scientist Clinical Pathology & Safety Biomarkers Resume Examples & Samples

  • Oversight of rigorous quality control procedures
  • Use and maintenance of laboratory instrumentation
  • Oversight of ordering and procurement of supplies
  • Development and validation of new assays
  • Preparation of written validation and study reports
66

Senior Associate Scientist Resume Examples & Samples

  • Designing and conducting small-scale shake flask and bioreactor experiments for cell culture process optimization, which requires some flexible schedule/weekend work
  • Leading prototype runs at 200L scale for material generation and to test scale-up strategy
  • Investigating and manipulating cellular metabolism for process understanding and improvement
  • Evaluating process robustness and developing mitigation strategy for tech transfer and campaign support
  • Liaising closely with the cell line and downstream development groups for execution of projects
  • Overseeing laboratory activities including scheduling, equipment maintenance, and vendor communication
  • Initiating and leading new technology assessment including external collaborations
  • .Writing technical summaries and development reports for efficient knowledge management
67

Scientist / Senior Associate Scientist Resume Examples & Samples

  • Evaluate/execute company’s current platforms and technologies in upstream and downstream process development
  • Participate in the technology transfer of bioprocesses internally and externally. The work will involve working with commercial and clinical production facilities to ensure accurate technology transfer and successful large-scale production
  • Generate, manage, interpret, and maintain critical data in a highly organized manner; write and present technical reports to management
  • Lead/participate in instrument purchasing and equipment maintenance for process development labs
  • Demonstrate effectiveness in collaborative projects in a matrix organization
  • Experience with developing fed-batch bioreactor processes including optimizing feeding strategies and evaluating different cell culture media and feed formulations
  • Development of robust, scalable, cost effective and well-characterized processes for
68

Senior Associate Scientist Resume Examples & Samples

  • Project Leadership and Collaboration
  • Lead project initiatives to ensure consistency of project objectives and technical strategies with business goals and to deliver R&D objectives in a timely manner by
  • At least Bachelor's Degree in Food/Nutrition related field. Master's Degree is preferable
  • At least 3 years of experience in the relevant role
  • High level of technical skills
  • Strong ability to lead several programs concurrently
  • Ability to leverage and collaborate with global technology resources in the business units
69

Senior Associate Scientist Assay Development Resume Examples & Samples

  • Pharmaceutical/biotechnology industry experience in basic drug discovery research
  • Familiarity with molecular biology, physiology & pharmacology of diverse target classes and an ability to resolve scientific & technical challenges on early-stage drug discovery projects
  • Proven expertise in protein & cellular reagent generation & qualification as well as broad experience in the development & implementation of cell-based (e.g., second messenger, reporter gene) and biochemical (e.g., radioligand binding, protein-protein interaction, enzymatic activity) assays in 384- or 1536-well microtiter plate format
  • Hands-on experience in the advanced operation of fluorescence/luminescence microtiter plate readers (e.g., FLIPR, EnVision, TopCount) and automated liquid handling systems (e.g., Bravo, Vprep, Echo, Washer/Dispenser II) in the context of HTS, hit characterization & lead optimization for multiple target classes
  • Experience using HTS-related data analysis software such as Screener, Spotfire, Pipeline Pilot
  • Ability to execute high quality experiments independently and to explain & communicate results to team colleagues while paying attention to project timelines & priorities
  • Highly motivated & enthusiastic team player demonstrating flexibility, a willingness to learn & a great sense of urgency
  • Excellent organizational, interpersonal as well as verbal & written communication skills
70

Senior Associate Scientist Resume Examples & Samples

  • Biochemical assay design and implementation
  • Cellular assay design and implementation
  • Assay optimization for high throughput screening
  • Molecular biology/cloning to support systems proteomics group
  • Tissue culture and cell maintenance
  • Tissue culture experience
  • Familiarity with high throughput screening
  • Molecular biology experience
  • Experience with FACS analysis
  • Working knowledge of CRISPR/Cas9
  • Solid foundation of biochemical knowledge
  • Knowledge of ubiquitin-proteosome system
  • Proteomic data analysis
  • Familiarity with gene-disease association databases
  • Experience with co-IP
71

Senior Associate Scientist Resume Examples & Samples

  • Master in biochemical engineering, biochemistry, pharmaceutical analysis, analytical chemistry or related disciplines, with >3 years’ experience in biopharmaceutical industry; or Ph.D in the same majors with 0-3 years’ experience in biopharmaceutical industry
  • Hands-on experiences in HPLC and CE methods for biopharmaceutics
  • Experiences in other analytical techniques and/or in GMP regulated environment is a plus
  • Fluent in English writing and speaking
  • Capable to obtain, interpret and present experimental results in a scientific manner
  • Self-motivated for personal development.1700160257W
72

Senior Associate Scientist Resume Examples & Samples

  • Support life cycle management of raw materials used in the clinical and commercial supply chain including Bill of Materials Assessment and other activities supporting raw material readiness as part of tech transfer to both internal and external manufacturing sites
  • Technical assessment of supplier-initiated and CMO-initiated changes
  • In close collaboration with API and DP technical teams, formulate characterization plans to advance understanding of raw materials in manufacturing processes and formulations including
  • Design, execution and/or lead designed experiments in support of raw material qualification
  • A Bachelors in Chemistry, Biology, Materials Science and Engineering, Biochemical Engineering, Chemical Engineering, Pharmacy/Pharmaceutics with at least 8 years of industrial experience OR a MS with at least 4 years of industrial experience is required
  • Demonstrated competency in effective written and verbal communication and good documentation practices are required
  • Demonstrated competency and experience in development and management of raw materials specifications including compendia testing is requuired
  • Demonstrated scientific contributions to the selection, use and qualification of raw materials for biological products – notably cell culture media, excipients and adjuvants - are preferred
  • Demonstrated competency and experience in use of project management tools (e.g., MS Project), spreadsheet and databases are required
  • Demonstrated experience is lean and/or six sigma methodologies and tools is preferred9295170503
73

Senior Associate Scientist Pdms Lm-ad Cork Resume Examples & Samples

  • Co-ordination and execution of routine release and stability testing Separations Methods for pre-clinical and clinical product development
  • Co-ordination and execution of Analytical Technology Transfer activities
  • Testing to support assay validation/qualification and other studies
  • Review and interpretation of Laboratory generated data
  • Review operation and maintenance of laboratory equipment
  • Completion of documentation in adherence to GMP
  • Participates in Technical discussions with with LM-AD Method development group
  • Support the maintenance of a GMP compliant laboratory
  • Lead continuous improvement projects
  • Supports troubleshooting and manages laboratory investigations
  • Perform Data Trending to support investigations, demonstrate method capability and product profile
  • Write SOP’s, protocols, work instructions and training modules
  • Other duties as assigned by team lead
  • Proven Separations expertise particularly with size exclusion and capillary methodologies
  • Experience with Method Development/Transfer/ Validation would be advantageous
  • Ability to work well within team structures and provide leadership
  • A minimum of a Degree in Molecular Biology, Biochemistry, Pharmacy or related scientific field is required
  • A minimum of 3 years analytical laboratory experience in a GLP/GMP environment
  • Knowledge of computer systems/programs e.g Empower, MS Word, Excel
  • Good understanding of quality and attention to detail.1700168386W
74

Senior Associate Scientist Resume Examples & Samples

  • Develop and execute bioanalytical assays, including LC-MSMS and ligand binding assays (LBA), for PK and exposure assessment of biotherapeutics
  • Develop in vitro assays for profiling of biotransformation and identify possible mechanisms, and establish in vitro- in vivo correlation, including affinity capture techniques
  • Develop quantitative assays for target assessment including expression level, turnover, and engagement
  • Work with experts of other technologies, such as flow cytometry and imaging, to establish an understanding of the disposition and key molecular attributes that contribute to distribution and clearance
  • Evaluate new technologies and instrumentation based on portfolio support needs
75

Senior Associate Scientist Resume Examples & Samples

  • Maintain mammalian cell culture and perform various cell-based assays to evaluate small-molecule chemical matter
  • Work within and support biology needs for drug discovery teams
  • Be positively engaged and have fun
  • Familiar with various cellular assays in high-throughput formats and automation equipment
  • Must have strong data handling skills including importing/exporting data into/from database, organizing data in an easy-to-interpret manner. Experience with a variety of scientific software applications is also required
76

Senior Associate Scientist Resume Examples & Samples

  • Develop and execute cell-based and biochemical assays to support project teams’ SAR efforts
  • Construct bacterial and baculovirus expression systems for recombinant proteins
  • Generate knockout, knockdown or enzymatically inactive target protein cell systems using approaches such as siRNA, shRNA and CRISPR for testing target validation hypotheses
  • Broadly trained in molecular and cell biology
  • Demonstrated ability to implement siRNA, shRNA and CRISPR technologies
  • Experience in designing and carrying out plate-based cell assays
  • An understanding of basic enzymolology
  • Experience with automated liquid handling systems is a very strong plus
  • Research experience in inflammatory & autoimmune diseases and/or cancer immunotherapy is a plus
  • Other Attributes
  • Ability to function independently within project teams
  • Ability to reliably execute on team responsibilities in a timely manner
  • Most importantly a positive, problem-solving can-do attitude
  • Resourceful
77

Senior Associate Scientist Resume Examples & Samples

  • Design and execute formulation development studies for small molecule and peptide drugs
  • Participate in oral solid dosage forms manufacturing processes development, process scale-up from bench top to pilot scale, technology transfer to commercial development and manufacturing organizations (CDMOs) and oversee clinical manufacturing campaigns at CDMOs. Manufacturing processes involve but not limited to granulation, encapsulation, tableting, coating, and spray drying
  • Design and execute pre-formulation studies to characterize solubility, ionization constant, lipophilicity, chemical stability, and-solid state properties of drug candidates. Testing includes but not limited to pharmaceutical powder characterization, pH measurement, HPLC, TGA, DSC, microscopy, dissolution, and XRPD
  • The incumbent will be responsible for compiling data, preparing summary presentation, and authoring technical reports. Effective communication skills are desirable for interaction with laboratory scientists and colleagues in a highly interdisciplinary and collaborative research and development environment
  • B.S./B.A. in Pharmaceutics, Chemical/Biochemical Engineering, Pharmacy, Biochemistry or related discipline with 5 years of industrial experience in pharmaceutical research and development environment
  • Hands-on experience in formulation and manufacturing process development of oral solid dosage forms for small molecules and peptides
  • Good understanding of physical, inorganic, and organic chemistry
  • Familiarity with FDA/ICH guidelines relative to drug substance and drug product development
78

Senior Associate Scientist Resume Examples & Samples

  • Development, optimization and validation of cell-based assays for biologic product lot release, stability, comparability, biosimilarity, reference standard qualification, and forced degradation studies
  • Transfer and maintenance of stable cell lines
  • Development of cell based assays with broad experience in microplate reader, fluorescence, luminescence, reporter gene, mesoscale, cell-based AlphaLISA, flow cytometry and FRET
  • Analysis of potency and parallelism of dose response curves using 4PL parameters and parallel-curve models, etc
  • Experience in design of experiment software (e.g., JMP)
  • Experience of molecular biology, including gene transcription, protein expression, qPCR, Western blotting, immunoprecipitation, etc
  • Documentation to support CGMP and regulatory filing
  • Provide assistance to project management to ensure meeting the requirements of project quality and timelines
  • Maintenance of instruments, and address technical and instrumental troubleshooting issues
  • Maintain study documentation
  • Meet regulatory compliance requirement
  • Maintain a safe work environment
79

Senior Associate Scientist Resume Examples & Samples

  • You are able to apply skills and knowledge to all stages of chemical synthesis. You support NME progression by supporting the establishment of health-based permitted daily exposure levels for INTs to assure quality production of APIs in facilities (i.e. pilot plants, manufacturing, etc.) where equipment is shared for the synthesis of numerous APIs (non-dedicated facilities). You support the classification of INTs in R&D based on hazards into a performance-based occupational exposure limit (PBOEL)
  • You support the management of intermediates testing, including technical review of draft protocols and study reports, help with program workflow (i.e. sample submission, certificates of analysis, outsourcing contracts, planning etc.), provide input on assay selection, work closely with CRO and aid in interpretation of study results. Stay current on global test-specific and REACH-like testing requirements
  • You manage daily functions and logistics of INTs testing, communicate with senior scientists any critical alert to help avoid negative impact on the submission and approval of new APIs
  • You assist senior scientists with necessary documentation and GMP requirements
  • You support Environment, Health, Safety and Sustainability by providing technical guidance to SDS authoring team in support of INTs hazard communication
  • You work reciprocally with internal groups (i.e. planning, outsourcing, SDS-authors, planning and outsourcing team, etc.) to increase efficiency and scientific integrity of assessments required. You are able to work collaboratively with external groups (i.e. CROs, vendors, etc.)
  • You seek training opportunities to demonstrate knowledge, continuous improvement and increase effectiveness of role
  • You support areas outside Janssen Occupational Toxicology/Product Quality as needed
  • Master’s Degree in Toxicology or related area is required
  • 4 years of relevant toxicology-related experience
  • Study monitoring experience is required
  • Experience working in a laboratory environment is required
  • Excellent written and oral communication skills in the English language is required
  • Be willing to look for training opportunities to build knowledge, to continuously improve and grow effectiveness
  • Willingness to advance the science of risk assessment, assay validation, etc
  • This position may require up to 10% domestic/international travel
80

Senior Associate Scientist Resume Examples & Samples

  • Basic laboratory experience with molecular biology required
  • Previous experience in animal handling, tissue collection, dosing required
  • Intricate survival surgeries (including stereotaxic) in adult and neonatal rodents required
  • Bachelor’s degree in science with minimum 12 years of working experience or Master’s with >5 years experience,
  • >3 years of experience with animal surgeries