About the role

Role Serve as a microbiology SME supporting GMP testing and lifecycle management of biopharmaceutical products at Bristol Myers Squibb. Responsibilitieslead method transfers validations verifications author and review GMP documentation investigate deviations, deviations, and CAPAs represent QC in audits and regulatory inspections drive continuous improvement initiatives mentor colleagues on microbiological methods manage data using LIMS and ELN systems
Requirements: Bachelor's in STEM (microbiology preferred) 10+ years of cGMP experience in biotechnology, cell therapy, or similar regulated environment proven expertise in microbiological testing, regulatory compliance, and quality systems prior ownership of cross-functional programs and project management skills High-Valuemicrobiology, GMP testing, method validation, microbiological investigations, regulatory audits, biotech or cell therapy products, lifecycle support.

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JOB OVERVIEW

Experience level

Lead

Location

Bothell, WA

Occupation

Microbiologists

Industry

Biological Product (except Diagnostic) Manufacturing

Posted

yesterday

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