Sr. Director, External Manufacturing Quality, Cell Therapy

Bristol Myers Squibb UK

Devens, MA, US
Base: $222,610 - $288,637 depending on location; b...
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Global cgmp compliance management
Cell therapy manufacturing oversight
Cmo and ctl relationship management
** Bristol Myers Squibb is seeking a Sr. Director of External Manufacturing Quality for their Cell Therapy division, responsible for defining quality strategies and ensuring compliance across global Contract Manufacturing Organizations. The ideal candidate will have extensive experience in quality compliance within the pharmaceutical industry and strong leadership abilities to manage teams and relationships with senior stakeholders. **

Job Summary

  • This role defines the Quality strategy for global Contract Manufacturing Organizations and ensures high-level cGMP compliance for Cell Therapy products.
  • The position requires leading a team to manage relationships with senior leaders in the CMO network and proactively improve quality performance through risk-based oversight.
  • Bristol Myers Squibb offers competitive benefits including health coverage, financial well-being programs, and flexible time off options.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Sr. Director of External Manufacturing Quality for their Cell Therapy division, responsible for defining quality strategies and ensuring compliance across global Contract Manufacturing Organizations. The ideal candidate will have extensive experience in quality compliance within the pharmaceutical industry and strong leadership abilities to manage teams and relationships with senior stakeholders. **

Salary

Base: $222,610 - $288,637 depending on location; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Comprehensive health, wellness, and paid time off included

Skills & Requirements

Must-have

  • Global cGMP compliance management
  • Cell Therapy manufacturing oversight
  • CMO and CTL relationship management
  • Quality Risk Management techniques
  • Health Authority inspection support
  • Strategic quality planning

Nice-to-have

  • Matrix environment leadership experience
  • Virtual Plant Team collaboration
  • Succession planning and talent development
  • Operational excellence deployment
  • High-performance culture building

Key Requirements

  • Minimum 15 years managing Quality and Compliance organizations
  • Bachelor's degree in science or pharmaceutical field required
  • Advanced degree preferred
  • Mastery of global cGMP/GDP regulations
  • Experience with CAR T and Gene Editing technologies

Work Rights

Not specified

Tailored Resume

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