Associate Director, Cell Therapy Network Cqv

Bristol Myers Squibb

Devens, MA, US
Base: $164,260 - $218,947; bonus/equity: + incenti...
Hybrid (50% onsite)
Cell therapy manufacturing gmp support
Cmc regulatory requirements
Validation lifecycle frameworks
Bristol Myers Squibb is seeking an Associate Director for their Cell Therapy Network CQV, responsible for establishing strategies for equipment and facility validation across the network. The ideal candidate will have extensive experience in cell therapy GMP manufacturing support and a strong understanding of regulatory requirements

Job Summary

  • The Associate Director, Cell Therapy Network CQV is responsible for the network strategy for equipment/facility/utility Commissioning, Qualification, and Validation.
  • This role will partner cross-functionally with site CQV leads, site equipment owners, Cell Therapy network Digital Plant leaders, and other key stakeholders.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director for their Cell Therapy Network CQV, responsible for establishing strategies for equipment and facility validation across the network. The ideal candidate will have extensive experience in cell therapy GMP manufacturing support and a strong understanding of regulatory requirements.

Salary

Base: $164,260 - $218,947; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Cell Therapy manufacturing GMP support
  • CMC regulatory requirements
  • validation lifecycle frameworks
  • equipment qualification and validation
  • GxP compliance

Nice-to-have

  • strategic thinking and problem-solving
  • project management tools
  • Lean Six Sigma tools
  • interpersonal and collaborative skills

Key Requirements

  • 15+ years w/ B.S. or 12 years w/ M.S. or 8 years w/ Ph.D. experience
  • B.S., M.S., or Ph.D. in Engineering or related discipline
  • Strong understanding of biologics or cell therapy GMP manufacturing
  • Strong understanding of DS & DP manufacturing
  • Strong understanding of analytical testing

Work Rights

Not specified

Tailored Resume

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