Senior Director, Product Quality Engineering

Bristol Myers Squibb

Devens, MA, US
Base: $223,640 - $298,092 depending on location; b...
50% onsite
12-15+ years gmp quality experience
7+ years people management in matrixed environment
5+ years cell/gene therapy manufacturing support
This role leads a global team dedicated to ensuring the highest standards of cGMP compliance and regulatory readiness across the cell therapy portfolio

Job Summary

  • This role leads a global team dedicated to ensuring the highest standards of cGMP compliance and regulatory readiness across the cell therapy portfolio.
  • The Senior Director is accountable for defining and implementing a global harmonization roadmap for quality standards, processes, and tools across all sites.
  • Bristol Myers Squibb offers competitive benefits including health coverage, financial well-being programs, and flexible time off options.

Matching Summary

This role leads a global team dedicated to ensuring the highest standards of cGMP compliance and regulatory readiness across the cell therapy portfolio.

Salary

Base: $223,640 - $298,092 depending on location; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellbeing support

Skills & Requirements

Must-have

  • 12-15+ years GMP Quality experience
  • 7+ years people management in matrixed environment
  • 5+ years cell/gene therapy manufacturing support
  • Deep knowledge of cGMP compliance and regulatory requirements
  • Experience with Integrated Control Strategy (ICS)
  • Track record of leading global quality teams

Nice-to-have

  • Experience with autologous CAR T cell therapy
  • Viral vector manufacturing background
  • Product launch and BLA submission support
  • Process digitization within quality operations
  • Quality control equipment automation experience
  • Culture of innovation and agility

Key Requirements

  • BS, MS, or PhD in Life Sciences
  • 12-15+ years experience in GMP Quality
  • 7+ years in people management
  • 5+ years supporting cell therapy or gene therapy
  • Demonstrated experience in global matrixed environments

Work Rights

Not specified

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