Associate Director, Aseptic & Sterile Process Engineering

Bristol Myers Squibb

Devens, MA, US
Base: $170,650 - $206,793; bonus/equity: + incenti...
50% onsite
8 years pharmaceutical manufacturing experience
Aseptic process simulation media fill expertise
Contamination control strategy development
Bristol Myers Squibb is seeking an Associate Director for Aseptic & Sterile Process Engineering to lead aseptic processing strategies in their advanced cell therapy manufacturing environment. The ideal candidate will possess significant experience in aseptic processing and regulatory readiness, with strong leadership skills to navigate a matrixed organization. This role offers opportunities for professional growth and a supportive work culture with competitive benefits

Job Summary

  • This role serves as a technical authority defining aseptic processing strategies for an advanced automated cell therapy manufacturing platform.
  • The position requires leading Aseptic Process Simulations (media fills) and ensuring inspection readiness for commercial filings and regulatory approvals.
  • Bristol Myers Squibb offers competitive benefits including flexible time off, health coverage, and a supportive culture focused on transforming patients' lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director for Aseptic & Sterile Process Engineering to lead aseptic processing strategies in their advanced cell therapy manufacturing environment. The ideal candidate will possess significant experience in aseptic processing and regulatory readiness, with strong leadership skills to navigate a matrixed organization. This role offers opportunities for professional growth and a supportive work culture with competitive benefits.

Salary

Base: $170,650 - $206,793; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • 8 years pharmaceutical manufacturing experience
  • Aseptic process simulation media fill expertise
  • Contamination control strategy development
  • Regulatory inspection support experience
  • Cleanroom qualification knowledge

Nice-to-have

  • Experience with automated robotic systems
  • Strong cross-functional matrix influence
  • Familiarity with mechanical sterile connectors
  • Advanced degree in engineering or science
  • Vendor management for technology developers

Key Requirements

  • Bachelor's degree in Engineering or related field
  • Minimum 8 years in biologics or cell therapy manufacturing
  • Direct experience leading media fill simulations
  • Proven track record supporting regulatory inspections

Work Rights

Not specified

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