Senior Specialist, Quality Assurance Shop Floor, Cell Therapy

Bristol Myers Squibb UK

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 for Quality Assurance on the Shop Floor in Devens, MA, focusing on cell therapy operations. The role involves providing oversight to manufacturing and quality control processes, ensuring compliance with policies and regulations in a dynamic environment. **

Job Summary

  • This position provides 24x7 Quality collaboration and oversight of site operations including Manufacturing, Quality Control laboratories, and Warehouse Operations.
  • The role requires identifying departures from approved procedures, reviewing records for compliance, and independently resolving complex quality issues.
  • Employees will work a rotating 2-3-2 Panama schedule and receive competitive benefits including health coverage, financial protection, and paid time off.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Specialist for Quality Assurance on the Shop Floor in Devens, MA, focusing on cell therapy operations. The role involves providing oversight to manufacturing and quality control processes, ensuring compliance with policies and regulations in a dynamic environment. **

Salary

Base: $89,780 - $108,789; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Health coverage, 401(k), paid time off, and global shutdown eligibility

Skills & Requirements

Must-have

  • 4+ years cGMP experience
  • Manufacturing site experience
  • FDA/EMA regulatory knowledge
  • Quality management systems
  • Electronic system proficiency

Nice-to-have

  • Cell therapy manufacturing background
  • Risk assessment expertise
  • Change control subject matter expert
  • Strong negotiation skills
  • Pioneering mindset

Key Requirements

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

Work Rights

Not specified

Tailored Resume

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