Director, Cell Therapy Quality Automation

Bristol Myers Squibb

Devens, MA, US
Devens - ma - us: $201,430 - $244,089; madison - g...
50% onsite
Cell therapy quality processes
Next-generation quality processes
Automated processing integration
This global position is responsible for the planning, execution, and implementation of next-generation quality processes to support high volume manufacturing processes

Job Summary

  • This global position is responsible for the planning, execution, and implementation of next-generation quality processes to support high volume manufacturing processes.
  • The Director will be a core member of critical cross-functional teams which identifies the future state cell therapy value stream in conjunction with automated processing.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

This global position is responsible for the planning, execution, and implementation of next-generation quality processes to support high volume manufacturing processes.

Salary

Devens - MA - US: $201,430 - $244,089; Madison - Giralda - NJ - US: $188,250 - $228,114; New Brunswick - NJ - US: $188,250 - $228,114; Princeton - NJ - US: $188,250 - $228,114; Seattle - WA: $207,080 - $250,929; Bonus/Equity: Additional incentive cash and stock opportunities (based on eligibility) may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Cell therapy quality processes
  • Next-generation quality processes
  • Automated processing integration
  • Advanced technologies and methodologies
  • Quality systems robustness and efficiency

Nice-to-have

  • Culture of innovation
  • Continuous improvement
  • Life-changing patient impact
  • Work-life balance and flexibility

Key Requirements

  • 14+ years of experience
  • Bachelor's degree in Engineering or Life Sciences
  • Strong knowledge of industry standards and regulatory requirements
  • Excellent leadership, communication, and project management skills
  • Ability to work collaboratively with cross-functional teams

Work Rights

Not specified

Tailored Resume

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