Deviation Jobs

Eurofins is hiring an on-site Process Engineer to manage GMP documentation, support sterile formulation and filling activities, and lead change control and deviation investigations for clinical product manufacturing.

At Elanco's Winslow manufacturing site, the Quality Assurance Associate will ensure product and process quality by managing deviations, supporting batch disposition, and driving compliance across operations.

Bristol Myers Squibb seeks a Specialist, Investigations to lead deviation investigations and CAPA activities within its cGMP cell therapy manufacturing site in Devens, MA.

Experienced quality compliance leader needed to own GxP inspection readiness, vendor audits, and quality system oversight at Rezolute's Redwood City office.

Penumbra is hiring a Quality Monitoring & Improvement Specialist I to support CAPA, NCR, and DA processes, coordinate board reviews, compile quality trending data, and assist with audits at the Alameda site.

Orca Bio is hiring a 2nd-shift Supervisor, Clinical Manufacturing to oversee on-site cell therapy production in Sacramento, ensuring quality, compliance, and efficient shift operations.

Vertex is seeking a Senior QA Specialist (2nd shift, contract) to drive GMP-compliant product disposition and on‑floor quality oversight for cell and gene therapy drug product operations.

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Hims & Hers is hiring a Quality Systems Lot Disposition Specialist to oversee batch record review, lot disposition, and quality documentation for XeCare Pharmacy to ensure compliance with regulatory and company standards.

Lead critical cGMP manufacturing operations for Biogen's large-scale cell culture team by executing processes, coaching associates, and ensuring high-quality documentation and compliance.

Experienced QA professional needed to lead technical document reviews, investigations, and validation oversight at Catalent's St. Petersburg soft-gel manufacturing site.