Senior Specialist, Quality Assurance Shop Floor, Cell Therapy

Bristor Myers Squibb

Devens, MA, United States
Base: $89,780 - $108,789; bonus/equity: + incentiv...
On-site
Quality oversight of manufacturing operations
Cgmp compliance
Deviation assessment and approval
Bristol Myers Squibb is seeking a Senior Specialist for Quality Assurance on the Shop Floor in Cell Therapy at their Devens, MA location. The role involves overseeing compliance with quality standards in manufacturing and operational areas, requiring strong problem-solving and leadership skills

Job Summary

  • The Quality Assurance Shop Floor team provides 24x7 quality collaboration and oversight of site operations, including Manufacturing, Quality Control laboratories, and Warehouse Operations.
  • This position will oversee and partner with operational areas to ensure compliance with Bristol-Myers Squibb policies, standards, procedures, and Global cGMP.
  • 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: 85

Bristol Myers Squibb is seeking a Senior Specialist for Quality Assurance on the Shop Floor in Cell Therapy at their Devens, MA location. The role involves overseeing compliance with quality standards in manufacturing and operational areas, requiring strong problem-solving and leadership skills.

Salary

Base: $89,780 - $108,789; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • Quality oversight of manufacturing operations
  • cGMP compliance
  • Deviation assessment and approval
  • Procedural document review and approval
  • Cross-functional collaboration

Nice-to-have

  • Pioneering mindset
  • Motivate and foster positive team environment
  • Negotiate and influence solutions

Key Requirements

  • Bachelor's degree in STEM field preferred
  • 4+ years of relevant cGMP experience
  • 1+ year of manufacturing site experience
  • Experience in FDA/EMA regulations
  • Demonstrated experience with quality management systems
  • Demonstrated experience with electronic systems and databases

Work Rights

Not specified

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