Senior Specialist, Quality Assurance Shop Floor, Cell Therapy

Bristol Myers Squibb

Devens, MA, US
Base: $89,780 - $108,789; bonus/equity: + incentiv...
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4+ years cgmp experience
Manufacturing site experience
Fda/ema regulatory knowledge
** Bristol Myers Squibb is seeking a Senior Specialist in Quality Assurance on the Shop Floor for their Cell Therapy operations in Devens, MA. The role involves overseeing compliance with quality standards in manufacturing and laboratory operations, requiring significant experience in cGMP and biopharmaceuticals. **

Job Summary

  • This role provides 24x7 quality collaboration and oversight of manufacturing, QC laboratories, and warehouse operations to ensure compliance with global cGMP standards.
  • The position requires independent identification of procedural departures, approval of temporary procedures, and leadership of cross-functional meetings to drive quality improvements.
  • Bristol Myers Squibb offers a competitive salary range of $89,780 - $108,789 along with comprehensive benefits including health coverage, 401(k) plans, and flexible time off options.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Specialist in Quality Assurance on the Shop Floor for their Cell Therapy operations in Devens, MA. The role involves overseeing compliance with quality standards in manufacturing and laboratory operations, requiring significant experience in cGMP and biopharmaceuticals. **

Salary

Base: $89,780 - $108,789; 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

  • 4+ years cGMP experience
  • Manufacturing site experience
  • FDA/EMA regulatory knowledge
  • Rotating Panama shift schedule
  • Quality management systems expertise

Nice-to-have

  • Cell therapy manufacturing background
  • Electronic system proficiency (MES/ERP)
  • Risk assessment subject matter expertise
  • Strong negotiation and influence skills
  • Pioneering mindset for innovation

Key Requirements

  • Bachelor's degree in STEM field preferred
  • 4+ years relevant cGMP experience required
  • Experience with FDA/EMA regulations in biopharma
  • Demonstrated experience with electronic databases like MES and ERP

Work Rights

Not specified

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