Sr. Director, External Manufacturing Quality, Cell Therapy

Bristol Myers Squibb

Devens, Massachusetts, United States
Base: $238,200 - $288,637 (devens ma); base: $222,...
Hybrid (50% onsite)
15+ years managing quality and compliance organizations
Deep mastery of global cgmp/gdp regulations
Experience with cell therapy and gene editing manufacturing
Bristol Myers Squibb is seeking a Sr. Director for External Manufacturing Quality in Cell Therapy, responsible for shaping the quality strategy for global manufacturing organizations. The role emphasizes compliance with cGMP standards and involves leading a team to enhance quality performance and build strong relationships across various stakeholders

Job Summary

  • This role defines the Quality strategy for global Contract Manufacturing Organizations and ensures high-level cGMP compliance for externally manufactured commercial cell therapy products.
  • The successful candidate will lead a team of Quality Senior Directors to manage the External Manufacturing Network, including CAR-T manufacturing and evolving Gene Editing technologies.
  • Bristol Myers Squibb offers competitive benefits including health coverage, financial well-being protection, and flexible time off options for eligible employees.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Sr. Director for External Manufacturing Quality in Cell Therapy, responsible for shaping the quality strategy for global manufacturing organizations. The role emphasizes compliance with cGMP standards and involves leading a team to enhance quality performance and build strong relationships across various stakeholders.

Salary

Base: $238,200 - $288,637 (Devens MA); Base: $222,610 - $269,747 (Madison NJ); Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Comprehensive health, wellness, and financial protection plans included

Skills & Requirements

Must-have

  • 15+ years managing Quality and Compliance organizations
  • Deep mastery of global cGMP/GDP regulations
  • Experience with Cell Therapy and Gene Editing manufacturing
  • Proven track record in CMO and CTL network oversight
  • Strong background in Quality Risk Management techniques

Nice-to-have

  • Excellent communication and interpersonal skills
  • Ability to build strong trusting relationships
  • Experience leading large complex programs
  • High business acumen and strategic thinking
  • Adaptability to changing work environments

Key Requirements

  • Minimum bachelor's degree in science or pharmaceutical related fields
  • >15 years of experience managing Quality and Compliance organizations
  • Advanced degree preferred
  • Mastery of global Quality compliance processes and regulations

Work Rights

Not specified

Tailored Resume

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