Vice President, Cell Therapy Global Quality

Bristol Myers Squibb UK

Base: $381,440 - $462,213; bonus/equity: + incenti...
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20+ years leadership experience in quality
Cell/gene therapy manufacturing expertise
Global gxp regulatory compliance knowledge
** Bristol Myers Squibb is seeking a Vice President for Cell Therapy Global Quality who will lead and optimize the quality organization for their global cell therapy network. The role involves overseeing compliance, quality assurance, and quality control processes while fostering an environment of engagement and growth within the team. **

Job Summary

  • This role is accountable for the development, deployment, and execution of the Quality strategy for the Cell Therapy Development and Cell Therapy Operations organizations globally.
  • The position requires leading a large workforce across multiple international sites including Summit NJ, Seattle WA, Leiden NE, Boudry CH, and Japan to ensure cGMP compliance.
  • Bristol Myers Squibb offers competitive benefits including health coverage, financial well-being programs, and flexible time off options for eligible employees.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Vice President for Cell Therapy Global Quality who will lead and optimize the quality organization for their global cell therapy network. The role involves overseeing compliance, quality assurance, and quality control processes while fostering an environment of engagement and growth within the team. **

Salary

Base: $381,440 - $462,213; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Comprehensive health, wellbeing, and financial protection plans included

Skills & Requirements

Must-have

  • 20+ years leadership experience in quality
  • Cell/Gene Therapy manufacturing expertise
  • Global GxP regulatory compliance knowledge
  • Health authority inspection management
  • Multi-site quality organization leadership

Nice-to-have

  • Innovative digital quality solutions
  • Strategic partnership with regulators
  • High-performance culture building
  • Advanced IT implementation skills
  • Cross-functional matrix collaboration

Key Requirements

  • BS degree in Science or Engineering; Advanced degree preferred
  • 20+ years relevant leadership experience in quality
  • Experience in Biologics or Cell/Gene Therapy manufacturing
  • Deep understanding of global regulatory requirements and guidelines
  • Proven track record in talent development and succession planning

Work Rights

Not specified

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