Specialist, Associate Process Engineer, Cell Therapy In Devens, Ma

Bristol Myers Squibb

Devens, MA, United States
Base: $79,150 - $95,914; bonus/equity: + incentive...
50% onsite
Gmp environment manufacturing support
Troubleshoot process and equipment issues
Deviation investigation and closure
The Specialist, Associate Process Engineer, Cell Therapy provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment, including troubleshooting process and equipment related issues

Job Summary

  • The Specialist, Associate Process Engineer, Cell Therapy provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment, including troubleshooting process and equipment related issues.
  • Responsibilities include facilitating deviation prevention and closure, analyzing manufacturing data, owning change controls, authoring SOPs, and participating in technology transfer efforts.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and emphasizes work-life balance, with opportunities for growth and a commitment to transforming patients' lives through science.

Matching Summary

The Specialist, Associate Process Engineer, Cell Therapy provides technical support to the Devens Cell Therapy Facility (CTF) Manufacturing processes in a GMP environment, including troubleshooting process and equipment related issues.

Salary

Base: $79,150 - $95,914; 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

  • GMP environment manufacturing support
  • Troubleshoot process and equipment issues
  • Deviation investigation and closure
  • Process improvement initiatives
  • Technology transfer participation
  • SOP authoring and revision

Nice-to-have

  • Continuous improvement tools application
  • Cross-functional team collaboration
  • Equipment and systems validation support
  • Patient-focused work environment

Key Requirements

  • BSc and/or MSc degree in Science or Chem/Bio Engineering
  • 0-3 years of industry experience
  • cGMP and/or Cell Therapy manufacturing experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter