Validation Engineer

Bristol Myers Squibb

Bothell, WA, US
Base: $83,220 - $100,847; bonus/equity: + incentiv...
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Gmp asset management and validation experience
Equipment qualification iq oq pq deliverables
Computer systems validation csv knowledge
** Bristol Myers Squibb is seeking a Validation Engineer for their Bothell, WA location, focusing on ensuring compliance with GMP regulations and validation processes in a regulated manufacturing facility. The ideal candidate will have a background in life sciences or engineering, with at least two years of relevant experience and a strong understanding of validation lifecycle deliverables. **

Job Summary

  • The Validation Engineer will play a critical role in ensuring compliance with all regulatory requirements and industry standards related to GMP asset management.
  • This position requires a hands-on validation engineer with experience in GMP, an understanding of lab/manufacturing equipment, and a proven track record in validation processes.
  • 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: 75

** Bristol Myers Squibb is seeking a Validation Engineer for their Bothell, WA location, focusing on ensuring compliance with GMP regulations and validation processes in a regulated manufacturing facility. The ideal candidate will have a background in life sciences or engineering, with at least two years of relevant experience and a strong understanding of validation lifecycle deliverables. **

Salary

Base: $83,220 - $100,847; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health coverage, 401(k), paid time off, and wellbeing support

Skills & Requirements

Must-have

  • GMP asset management and validation experience
  • Equipment qualification IQ OQ PQ deliverables
  • Computer systems validation CSV knowledge

Nice-to-have

  • Cell therapy industry background preferred
  • Risk-based validation approach implementation
  • Cross-functional team collaboration skills

Key Requirements

  • Bachelor's Degree in life sciences/engineering/STEM
  • 2+ years of commissioning qualification and validation CQV experience
  • Experience in Pharma/Biopharma required

Work Rights

Not specified

Tailored Resume

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