Senior Specialist, Validation Engineer Ii

Bristol Myers Squibb

Devens, MA, US
Base: $92,540 - $112,136; bonus/equity: + incentiv...
**
Bachelor of science in engineering required
3+ years fda regulated manufacturing experience
2+ years equipment or utility qualification
** Bristol Myers Squibb is seeking a Senior Specialist, Validation Engineer II to support the implementation of manufacturing and laboratory equipment at their Devens, MA facility. The ideal candidate will have experience in qualification and validation processes in the pharmaceutical industry, and the role offers a hybrid work environment with competitive benefits. **

Job Summary

  • The role supports the successful implementation of manufacturing and laboratory equipment alongside facilities and utilities at multi-use sites.
  • Candidates will develop and execute validation deliverables such as Validation Plans, Requirements Specifications, and Traceability Matrices while adhering to strict deadlines.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being protection, and flexible time off options.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Specialist, Validation Engineer II to support the implementation of manufacturing and laboratory equipment at their Devens, MA facility. The ideal candidate will have experience in qualification and validation processes in the pharmaceutical industry, and the role offers a hybrid work environment with competitive benefits. **

Salary

Base: $92,540 - $112,136; 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

  • Bachelor of Science in Engineering required
  • 3+ years FDA regulated manufacturing experience
  • 2+ years equipment or utility qualification
  • Knowledge of cGMP and regulatory guidelines
  • Experience with validation lifecycle maintenance

Nice-to-have

  • Familiarity with lean principles and Six Sigma
  • Experience with GAMP automation validation
  • Background in biologics or cell therapy
  • Strong project management and communication skills
  • Ability to work independently on complex projects

Key Requirements

  • Bachelor of Science degree in Chemical or Mechanical Engineering
  • Minimum 3 years relevant experience in FDA regulated facility
  • Minimum 2 years experience in equipment, facility, or utility qualification

Work Rights

Not specified

Tailored Resume

Cover Letter