Automation Engineer I

Bristol Myers Squibb

Madison, NJ, US
Base: $100,100 - $121,293; bonus/equity: + incenti...
50% onsite
4+ years automation systems experience
Gmp environment system validation iq oq pq
21 cfr part 11 annex 11 compliance knowledge
This role serves as the system owner and lifecycle steward for integrated automation systems supporting analytical methods in late-stage and commercial cell therapy programs

Job Summary

  • This role serves as the system owner and lifecycle steward for integrated automation systems supporting analytical methods in late-stage and commercial cell therapy programs.
  • The position drives governance of technology transfers from Analytical Development into ASAT while ensuring systems remain validated and inspection-ready across GMP laboratories.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being protection, and flexible work-life balance options.

Matching Summary

This role serves as the system owner and lifecycle steward for integrated automation systems supporting analytical methods in late-stage and commercial cell therapy programs.

Salary

Base: $100,100 - $121,293; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Health coverage, 401(k), paid time off, and wellbeing support

Skills & Requirements

Must-have

  • 4+ years automation systems experience
  • GMP environment system validation IQ OQ PQ
  • 21 CFR Part 11 Annex 11 compliance knowledge
  • Automated analytical platform operation expertise
  • Technology transfer from development to commercial

Nice-to-have

  • Experience with Biosero or HighRes Biosolutions
  • Liquid handling and automation workflow programming
  • Familiarity with LIMS integration systems
  • Experience managing multiple automation vendors
  • Supporting regulatory inspections and audits

Key Requirements

  • BS or MS in engineering or related scientific discipline
  • Minimum 4 years of experience in regulated automation environments
  • Proven track record governing full validation lifecycle activities

Work Rights

Not specified

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