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Lead Manufacturing Associate, Cell Therapy in Devens, MA

Bristol Myers Squibb
September 29, 2026
Full-time
On-site
Devens, MA
Operations
Role: Lead Manufacturing Associate, Cell Therapy, supporting routine GMP manufacturing of cell therapy products. Responsibilities: perform process unit operations, maintain environmental conditions, document activities per SOPs, support equipment setup, and collaborate with cross-functional teams for process transfers and investigations. Requirements: 4+ years in cGMP bioprocessing or cell therapy manufacturing; Bachelor’s in relevant science or engineering; experience with cell washing, separation, cryopreservation, bioreactors, and aseptic processing; knowledge of FDA/gGMP standards. Preferred: experience working in BSL-2 environments, handling human blood components, and working with automated cell processing equipment. High-Value: biologics/cell therapy (likely autologous or allogeneic), GMP, aseptic processing, experience with cell expansion, cryopreservation, and bioreactors. Work setup: on-site in Devens, MA, with rotating shifts (days/nights, including holidays and weekends); physical requirements include standing, lifting up to 50 lbs, and PPE use.