Quality Control Microbiologist Resume Samples

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FK
F Kohler
Florian
Kohler
21460 Ezra Trace
Philadelphia
PA
+1 (555) 170 4348
21460 Ezra Trace
Philadelphia
PA
Phone
p +1 (555) 170 4348
Experience Experience
Phoenix, AZ
Quality Control Microbiologist
Phoenix, AZ
Osinski Group
Phoenix, AZ
Quality Control Microbiologist
  • Demonstrated proficiency in Aseptic Process Environmental Monitoring, Aseptic Testing, Microbial Monitoring, Gram Staining, Sub-culturing, Bacterial Endotoxin Testing, Bioburden Testing, TOC, Plating, Membrane Filtration, and other USP testing
  • Coordinate with Manager and other team members in organizing workload as to ensure timely release of all testing
  • Troubleshoot instrument problems and work with the lab supervisor/manager and equipment manufacturer’s technical services to resolve issues
  • Perform accurate and timely sterility testing per procedure and report results per cGMP/GLP Guidelines
  • Perform other duties as assigned
  • Schedule and perform QC activities in Blue Mountain RAM platform
  • Perform in-house microbiological assays, water, and steam attribute testing and other sampling procedures
Phoenix, AZ
Quality Control Microbiologist, nd Shift
Phoenix, AZ
Cummings Inc
Phoenix, AZ
Quality Control Microbiologist, nd Shift
  • Perform microbiological testing (endotoxin, bioburden) for water
  • Perform microbiological testing (endotoxin, sterility and bioburden) for raw materials, in-process materials, intermediates and final product
  • Perform environmental monitoring of the clean rooms (under ISO and EU specifications)
  • Perform line clear and line start verifications
  • Perform microbial characterization (gram stain, catalase, oxidase, and couagulase tests)
  • Perform other microbiological assays
  • Maintain historical files on organisms found in classified areas; microbial identification and trending
present
San Francisco, CA
Senior Quality Control Microbiologist
San Francisco, CA
Spencer-Ziemann
present
San Francisco, CA
Senior Quality Control Microbiologist
present
  • Perform analytical testing as a main priority with efficiency and accuracy
  • May provide technical guidance
  • Evaluate lab practices for compliance and operational excellence improvement on a continuous basis
  • Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays
  • Write protocols and perform assay validation and equipment qualification/verification
  • Report, evaluate, back-up/archive, trend and approve analytical data
  • Initiate and/or implement changes in controlled documents
Education Education
Bachelor’s Degree in Microbiology
Bachelor’s Degree in Microbiology
Pepperdine University
Bachelor’s Degree in Microbiology
Skills Skills
  • Excellent verbal and written communication skills Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls)
  • Able to use statistical analysis tools to perform data trending and evaluation
  • Project Management and organizational skills, including ability to follow assignments through to completion
  • Escalate issues professionally and on a timely basis
  • Applies research, information gathering, analytical, and interpretation skills to problems of diverse scope
  • Negotiation and Influence skills
  • Problem solving skills
  • Teamwork and Coaching others
  • Ensures compliance within regulatory environment
  • Develops solutions to technical problems of moderate complexity
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4 Quality Control Microbiologist resume templates

1

Senior Quality Control Microbiologist Resume Examples & Samples

  • Bachelor's degree in a science discipline
  • Biopharmaceutical QC experience in a microbiology lab
  • Experience in a wide variety of microbiological techniques, including but not limited to Bioburden, Endotoxin, Sterility (in an Isolator), Environmental Monitoring, Rapid Micro techniques, Microbial Identification, Media prep, Water Sampling
  • Understanding and application of principles, concepts, theories and standards of GMP QC microbiology laboratories. Deepens technical knowledge through exposure and continuous learning
  • Take initiative to identify and drive improvements
  • Excellent verbal and written communication skills Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls)
  • Escalate issues professionally and on a timely basis
  • Teamwork and Coaching others
  • Negotiation and Influence skills
  • Applies research, information gathering, analytical, and interpretation skills to problems of diverse scope
  • Ensures compliance within regulatory environment
  • Develops solutions to technical problems of moderate complexity
  • Screens, categorizes, evaluates, reconciles, reports, and resolves data integrity issues
  • Able to use statistical analysis tools to perform data trending and evaluation
  • Project Management and organizational skills, including ability to follow assignments through to completion
2

Associate Microbiologist Quality Control Resume Examples & Samples

  • Execute laboratory work, schedule with input from supervisor or senior team member
  • Drafts technical documents such as SOPs, COAs and protocols with direct supervision
  • Perform parallel review of laboratory documents, may perform technical review of documents such as protocols, specifications, etc
  • Perform parallel review, verification of actions and transcription
  • Trains, coaches or mentors on technical issues. Trains others on laboratory techniques
  • Executes Operational Excellence/efficiency projects with guidance
  • Bachelor’s Degree w/ 5+ years experience
  • Master’s Degree w/ 2+ years experience
3

Quality Control Associate Microbiologist Resume Examples & Samples

  • Test products as scheduled in an efficient and timely manner per procedures and specifications
  • Trouble shoot performance testing issues with the help of management and coworkers. Only forward lots to Industrialization after investigation into performance testing issues have been completed. Perform failure analysis at a level to determine preliminary cause of problem
  • Support product and process improvements
  • Support special projects as directed by management
  • Certified in organism subculture, and setting up reagents for performance testing
  • Update QC Database with lot status each day, and file Quality records routinely
  • Support Environmental Monitoring
  • Certified in Device History Review and Base Broth Book Reviews for GMP compliance per procedures and regulations
  • Take ownership of a product line for shelf life testing
  • Certified with Trackwise and initiate Nonconforming Material Reports (NCMR’s) and Nonconformance (NC’s)
  • Temporary modification to provide reasonable accommodations do not waive any essential functions of the job requirements
  • Reasonable, reliable attendance and punctuality is an essential job function required for this position
  • Must have a 4 year scientific college degree or equivalent
  • Experience in a microbiology lab is preferred
  • Provide technical review of QC data
  • Identify adverse trends and propose corrective actions
  • Knowledge of GMP compliance
  • Provide accurate, timely and reliable information and reports
  • Adhere & enforce bioMérieux quality policies and procedures
  • Support global quality initiatives
  • Knowledge of quality risk assessments and quality policies and procedures
  • Assist management to identify and mitigate gaps in quality systems
4

Quality Control Microbiologist, nd Shift Resume Examples & Samples

  • Knowledgeable in FDA cGMPs (21 CFR 211); ISO 9001, 13485 and 17025 a plus
  • Strong organizational skills and the ability to prioritize/multitask
  • Proficient in Microsoft Office Suite (excel)
5

Quality Control Microbiologist Resume Examples & Samples

  • Perform accurate and timely sterility testing per procedure and report results per cGMP/GLP Guidelines
  • Support all manufacturing and validation operations; including but not limited to process validation, environmental monitoring, and utility systems
  • Perform in-house microbiological assays, water, and steam attribute testing and other sampling procedures
  • Prepare analytical reports, trend analysis reports or yearly summaries as required
  • In a timely fashion, review, and release of microbiological test results as to ensure compliance with standard operating procedures
  • Oversee daily activities in the absence of the supervisor/manager
  • Troubleshoot instrument problems and work with the lab supervisor/manager and equipment manufacturer’s technical services to resolve issues
  • Perform instrument maintenance and calibration verification/standardization as required
  • Schedule and perform QC activities in Blue Mountain RAM platform
  • Initiate, investigate and write deviations, change controls, out of specification (OOS), out of trend (OOT)
  • Write, revise, and review standard operating procedures (SOPs) applicable to QC operations
  • Support domestic and international regulatory agency inspections
  • Mentor Microbiology staff on compendia, instrument operations, maintenance and test methods per SOPs, and agency regulations as needed
  • Coordinate with Manager and other team members in organizing workload as to ensure timely release of all testing
  • Must be able to work as part of a team and also independently with minimum supervision
  • Travel required to various local United Therapeutics facilities as necessary for assigned projects
  • Knowledge and understanding of cGMPs, USP, EP, JP, FDA, and other regulatory requirements
  • Experience working with LIMS systems
6

Quality Control Senior Microbiologist Resume Examples & Samples

  • Manage the transfer and provide technical oversight of Microbiological methods from Development to QC (validation of methods and tech transfer of methods, including comparability)
  • Establish user requirements for purchase, qualification of Kite’s QC equipment and work with internal and external resources to maintain equipment in an optimal state
  • Develop, revise and review SOPs, qualification/validation protocols and reports
  • Conduct investigations regarding out of specifications (OOS) results and address and manage deviations related to micro procedures
  • Monitor the GMP systems currently in place to ensure compliance with documented policies
  • Gather metric information for use in continuous improvement of areas of responsibility