Manager, Cell Therapy Manufacturing In Devens, Ma

Bristol Myers Squibb

Devens, MA, US
Base: $104,975 - $127,205; bonus/equity: + incenti...
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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, responsible for overseeing clinical and commercial product manufacturing. The role requires extensive experience in cGMP bioprocessing and cell therapy techniques, emphasizing compliance, safety, and team leadership. **

Job Summary

  • The role 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.
  • Candidates will lead the development of corrective and preventative actions while fostering a culture of safety and compliance to protect patients.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Manager for Cell Therapy Manufacturing in Devens, MA, responsible for overseeing clinical and commercial product manufacturing. The role requires extensive experience in cGMP bioprocessing and cell therapy techniques, emphasizing compliance, safety, and team leadership. **

Salary

Base: $104,975 - $127,205; Bonus/Equity: Additional 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 (implied by location)

Work Rights

Not specified

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