Associate Director, Aseptic Observation Program

Bristol Myers Squibb

Summit West, NJ, US
Base: $163,210 - $197,770; bonus/equity: + incenti...
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Aseptic processing principles
Contamination control strategies
Cgmp and regulatory environment
** Bristol Myers Squibb is seeking an Associate Director for its Aseptic Observation Program in Summit West, NJ. The role involves strategic leadership in aseptic practices within cleanroom environments, aiming to enhance operational excellence and compliance in a highly regulated industry. **

Job Summary

  • This leader will shape the operational culture from the ground up, ensuring the site is staffed with exceptional talent, achieves operational readiness on an aggressive timeline, and continuously delivers operational excellence in a highly regulated, patient-centric environment.
  • You will provide strategic leadership and direction for the team responsible for overseeing aseptic practices within Cell Therapy manufacturing cleanrooms and supporting environments.
  • 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

Match Score: 75

** Bristol Myers Squibb is seeking an Associate Director for its Aseptic Observation Program in Summit West, NJ. The role involves strategic leadership in aseptic practices within cleanroom environments, aiming to enhance operational excellence and compliance in a highly regulated industry. **

Salary

Base: $163,210 - $197,770; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Aseptic processing principles
  • Contamination control strategies
  • cGMP and regulatory environment
  • Operational excellence methodologies
  • Front line operator coaching

Nice-to-have

  • Building and scaling operations teams
  • Cross-functional collaboration
  • Adaptable to fast-paced environment
  • Data integrity requirements

Key Requirements

  • 8 – 12 years of experience in cGMP cell therapy manufacturing
  • Bachelors in relevant science or engineering discipline
  • Experience in aseptic processing in ISO 5/Grade A biosafety cabinets

Work Rights

Not specified

Tailored Resume

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