Senior Manager Quality Control Investigations

Bristol Myers Squibb

Devens, MA, US
Base: $124,590 - $150,977; bonus/equity: + incenti...
50% onsite
5-8 years qc laboratory experience
Root cause analysis expertise
Capa management in regulated environment
Bristol Myers Squibb is seeking a Senior Manager for Quality Control Investigations in Devens, MA, who will lead site investigations and corrective and preventive action (CAPA) execution related to quality control operations. The ideal candidate will have extensive experience in quality control and laboratory operations within the biotech or pharmaceutical industries, as well as strong expertise in regulatory compliance and investigation management

Job Summary

  • This role provides leadership and ownership for site investigations and CAPA execution related to QC operations and laboratory activities.
  • The position requires ensuring investigations are scientifically sound, timely, and compliant while partnering closely with Quality Assurance for independent oversight.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being programs, and flexible work-life balance options.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Manager for Quality Control Investigations in Devens, MA, who will lead site investigations and corrective and preventive action (CAPA) execution related to quality control operations. The ideal candidate will have extensive experience in quality control and laboratory operations within the biotech or pharmaceutical industries, as well as strong expertise in regulatory compliance and investigation management.

Salary

Base: $124,590 - $150,977; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Health, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • 5-8 years QC laboratory experience
  • Root cause analysis expertise
  • CAPA management in regulated environment
  • cGMP regulations and ICH guidelines knowledge
  • Data integrity principles application

Nice-to-have

  • Experience with Veeva or TrackWise systems
  • Laboratory informatics (LIMS) proficiency
  • Strong collaboration across cross-functional teams
  • Continuous improvement initiative drive

Key Requirements

  • Bachelor's degree in Life Sciences or related field
  • 5-8 years experience in GMP laboratory operations
  • Demonstrated expertise leading laboratory investigations

Work Rights

Not specified

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