Aseptic Process Validation Lead — Cell Therapy
Listed on 2026-09-30
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Pharmaceutical
Validation Engineer, Pharma Engineer, Pharmaceutical Manufacturing
Bristol Myers Squibb in Devens, MA, is seeking a Senior Specialist, Associate Aseptic Process Validation Engineer to support the Cell Therapy facility. You will contribute to aseptic process validation programs and help ensure manufacturing readiness.
The role emphasizes collaboration with MS&T and cross-functional teams, cGMP compliance, and readiness for regulatory inspections, with opportunities to impact patient outcomes through biotech innovations.
We have an opening for a Aseptic Process Validation Lead — Cell Therapy in MA, United States within Engineering.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Aseptic Process Validation Lead — Cell Therapy role in the description above.
We appreciate your interest in this position.
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