Manager, Cell Therapy Manufacturing In Devens, Ma

Bristol Myers Squibb

Devens, MA, US
Base: $104,975 - $127,205; bonus/equity: + incenti...
Hybrid (50% onsite)
5+ years cgmp bioprocessing experience
Cell therapy manufacturing techniques
Aseptic processing in iso 5 biosafety cabinets
Bristol Myers Squibb is seeking a Manager of Cell Therapy Manufacturing in Devens, MA, responsible for overseeing the manufacturing of clinical and commercial cell therapy products. The role emphasizes leadership in a cGMP-compliant environment, requiring strong technical skills and experience in bioprocessing

Job Summary

  • The Manager will support commercial operations by overseeing 24/7 shifts for cell therapy manufacturing units including media preparation and cell processing.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial protection, and flexible time off options.
  • This role requires maintaining a compliant environment while fostering a culture of safety, teamwork, and urgency to transform patients' lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager of Cell Therapy Manufacturing in Devens, MA, responsible for overseeing the manufacturing of clinical and commercial cell therapy products. The role emphasizes leadership in a cGMP-compliant environment, requiring strong technical skills and experience in bioprocessing.

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 experience
  • Shift work including holidays and weekends
  • Clean room environment work

Nice-to-have

  • Experience with automated equipment
  • Incubators and bioreactors operation
  • Cryopreservation processes
  • Team leadership and mentoring skills
  • Strong communication abilities

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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