Specialist, Quality Assurance Shop Floor

Bristor Myers Squibb

Devens, MA, United States
Base: $40.16 - $48.67 ph; bonus/equity: not specif...
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Quality oversight of site operations
Cgmp compliance
Manufacturing execution system (mes) documentation
** Bristol Myers Squibb is seeking a Specialist for Quality Assurance on the shop floor in Devens, MA. The role involves ensuring compliance with quality standards and procedures within manufacturing and quality control environments, focusing on oversight and collaboration across operational areas. **

Job Summary

  • The Quality Assurance Shop Floor team is responsible for 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 our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Specialist for Quality Assurance on the shop floor in Devens, MA. The role involves ensuring compliance with quality standards and procedures within manufacturing and quality control environments, focusing on oversight and collaboration across operational areas. **

Salary

Base: $40.16 - $48.67 per hour; Bonus/Equity: Not specified; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Paid Time Off

Skills & Requirements

Must-have

  • Quality oversight of site operations
  • cGMP compliance
  • Manufacturing Execution System (MES) documentation
  • Review manufacturing batch records
  • Approve deviation records
  • Work in cleanroom environments

Nice-to-have

  • Action-oriented decision-making
  • Problem-solving and analytical thinking
  • Build and maintain relationships
  • Champion for quality culture

Key Requirements

  • 2+ years of relevant cGMP experience
  • 1+ year of manufacturing site experience
  • Bachelor's degree in STEM field or equivalent experience
  • Experience in FDA/EMA regulations

Work Rights

Not specified

Tailored Resume

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