Associate Director, Aseptic & Sterile Process Engineering

Bristol Myers Squibb

Devens, MA, United States
Devens - ma - us: $170,650 - $206,793; not specifi...
On-site
Aseptic processing strategy
Contamination control strategy
Aseptic process simulation
Bristol Myers Squibb is seeking an Associate Director of Aseptic & Sterile Process Engineering in Devens, MA, to lead aseptic processing strategies for advanced automated manufacturing in cell therapy. The ideal candidate will have extensive experience in aseptic processing and contamination control, with a strong ability to influence cross-functional teams

Job Summary

  • The Associate Director will serve as a technical leader for aseptic and sterile processing strategy supporting an advanced, automated manufacturing platform for cell therapy.
  • This role is responsible for defining, justifying, and sustaining aseptic processing strategies that support regulatory approval and long-term commercial manufacturing.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director of Aseptic & Sterile Process Engineering in Devens, MA, to lead aseptic processing strategies for advanced automated manufacturing in cell therapy. The ideal candidate will have extensive experience in aseptic processing and contamination control, with a strong ability to influence cross-functional teams.

Salary

Devens - MA - US: $170,650 - $206,793; Not specified; Health Coverage: Medical, pharmacy, dental, and vision care.

Skills & Requirements

Must-have

  • aseptic processing strategy
  • contamination control strategy
  • aseptic process simulation
  • regulatory inspection readiness
  • automation and equipment design integration

Nice-to-have

  • advanced manufacturing technologies
  • cross-functional leadership
  • risk-based justifications
  • emerging technologies evaluation

Key Requirements

  • Bachelor's degree in Engineering, Biotechnology, Pharmaceutical Sciences, Microbiology, or related scientific/technical discipline
  • Minimum of 8 years of experience in pharmaceutical, biologics, or cell and gene therapy manufacturing
  • Significant hands-on experience with aseptic processing and sterile manufacturing operations
  • Demonstrated experience with contamination control strategies, environmental monitoring, and cleanroom qualification
  • Direct experience leading or supporting Aseptic Process Simulations (media fills)
  • Experience supporting regulatory inspections, commercial readiness, or technology transfer activities

Work Rights

Not specified

Tailored Resume

Cover Letter