Manager, Cell Therapy Manufacturing In Devens, Ma

Bristol Myers Squibb

Devens, MA, US
Base: $104,975 - $127,205; bonus/equity: incentive...
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5+ years cgmp bioprocessing experience
Cell therapy manufacturing techniques
Aseptic processing in iso 5 biosafety cabinets
** Bristol Myers Squibb is seeking a Manager for Cell Therapy Manufacturing in Devens, MA, to oversee the production of clinical and commercial products in a cGMP-compliant environment. The role requires a strong background in bioprocessing and cell therapy manufacturing, along with leadership experience. **

Job Summary

  • The Manager supports commercial operations by overseeing shifts that cover 24/7 cell therapy manufacturing unit operations in accordance with Current Good Manufacturing Practices.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs to help employees pursue their goals both at work and in their personal lives.
  • This role requires working in a clean room environment with exposure to human blood components and close proximity to strong magnets.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Manager for Cell Therapy Manufacturing in Devens, MA, to oversee the production of clinical and commercial products in a cGMP-compliant environment. The role requires a strong background in bioprocessing and cell therapy manufacturing, along with leadership experience. **

Salary

Base: $104,975 - $127,205; Bonus/Equity: Incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off

Skills & Requirements

Must-have

  • 5+ years cGMP bioprocessing experience
  • Cell therapy manufacturing techniques
  • Aseptic processing in ISO 5 biosafety cabinets
  • BSL-2 containment area handling
  • Shift work including holidays and weekends

Nice-to-have

  • Experience with automated equipment
  • Strong teamwork and communication skills
  • Culture of safety and urgency
  • Mentoring and developing people

Key Requirements

  • Bachelor's degree in science or engineering
  • 5+ years experience in cGMP bioprocessing
  • US work authorization required for onsite role

Work Rights

Not specified

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