Senior Specialist, Quality Assurance Shop Floor, Cell Therapy

Bristol Myers Squibb

Devens, MA, US
Base: $89,780 - $108,789; bonus/equity: + incentiv...
50% onsite
4+ years cgmp experience
Cell therapy manufacturing knowledge
Fda/ema regulatory compliance
Bristol Myers Squibb is seeking a Senior Specialist for Quality Assurance on the Shop Floor in Devens, MA. The role involves overseeing compliance with quality standards in cell therapy manufacturing, requiring a strong background in cGMP and relevant experience in biopharmaceuticals

Job Summary

  • This role provides 24x7 quality collaboration and oversight of site operations including manufacturing, QC laboratories, and warehouse operations.
  • The position requires independent identification of departures from approved procedures and the ability to escalate critical issues while ensuring global cGMP compliance.
  • Bristol Myers Squibb offers a competitive benefits package including health coverage, financial protection, and flexible time off options.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Specialist for Quality Assurance on the Shop Floor in Devens, MA. The role involves overseeing compliance with quality standards in cell therapy manufacturing, requiring a strong background in cGMP and relevant experience in biopharmaceuticals.

Salary

Base: $89,780 - $108,789; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Comprehensive medical, dental, vision, 401(k), and paid time off

Skills & Requirements

Must-have

  • 4+ years cGMP experience
  • Cell therapy manufacturing knowledge
  • FDA/EMA regulatory compliance
  • Shift work availability (Panama schedule)
  • Manufacturing Execution Systems (MES) proficiency

Nice-to-have

  • Strong negotiation and influence skills
  • Experience with risk assessments
  • Ability to lead cross-functional meetings
  • Pioneering mindset for innovation
  • Training curriculum development experience

Key Requirements

  • Bachelor's degree in STEM field preferred
  • 4+ years relevant cGMP experience
  • 1+ year manufacturing site experience
  • Demonstrated experience with quality management systems
  • Proficiency with electronic databases like ERP/MES

Work Rights

Not specified

Tailored Resume

Cover Letter