Sr. Director, External Manufacturing Quality, Cell Therapy

Bristol Myers Squibb

Devens, MA, US
Base: $222,610 - $288,637 depending on location; b...
**
Global cgmp compliance management
External manufacturing organization leadership
Cell therapy product quality strategy
** Bristol Myers Squibb is seeking a Sr. Director of External Manufacturing Quality for Cell Therapy, responsible for defining the Quality strategy for global Contract Manufacturing Organizations (CMOs) and ensuring compliance with regulatory standards. The ideal candidate will have extensive experience in Quality and Compliance management, particularly in the pharmaceutical sector, and will play a crucial role in maintaining high-quality standards and improving CMO performance. **

Job Summary

  • This role defines the quality strategy for global Contract Manufacturing Organizations to ensure the safety and efficacy of externally manufactured commercial cell therapy products.
  • The position requires leading a team to manage quality assurance agreements, oversee audits, and resolve technical problems in alignment with global standards.
  • Bristol Myers Squibb offers competitive benefits including flexible time off, comprehensive health coverage, and opportunities for work-life balance in a supportive culture.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Sr. Director of External Manufacturing Quality for Cell Therapy, responsible for defining the Quality strategy for global Contract Manufacturing Organizations (CMOs) and ensuring compliance with regulatory standards. The ideal candidate will have extensive experience in Quality and Compliance management, particularly in the pharmaceutical sector, and will play a crucial role in maintaining high-quality standards and improving CMO performance. **

Salary

Base: $222,610 - $288,637 depending on location; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Health coverage, 401(k), paid time off, and wellbeing support programs

Skills & Requirements

Must-have

  • Global cGMP compliance management
  • External Manufacturing Organization leadership
  • Cell Therapy product quality strategy
  • CMO and CTL vendor oversight
  • Quality Risk Management techniques

Nice-to-have

  • Experience with virtual plant teams
  • Strong matrix environment negotiation skills
  • 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 related fields
  • Mastery of global cGMP/GDP regulations for External Manufacturing QA

Work Rights

Not specified

Tailored Resume

Cover Letter