Senior Manager, Quality Assurance Shop Floor 2nd Shift

Bristol Myers Squibb

Devens, MA, US
Base: $130,020 - $157,559; bonus/equity: + incenti...
50% onsite
Cgmp regulatory compliance expertise
Cell therapy manufacturing process knowledge
Night shift leadership and management
Bristol Myers Squibb is seeking a Senior Manager for Quality Assurance on the 2nd Shift at their Devens, MA facility. The role involves leading quality oversight for cell therapy manufacturing processes, managing night-shift teams, and fostering a culture of quality and compliance

Job Summary

  • This role serves as a key people leader ensuring the highest quality standards in cGMP Cell Therapy processes at the Devens facility.
  • The incumbent is responsible for leading two night-shift managers and their teams to uphold quality, compliance, and patient safety.
  • Bristol Myers Squibb offers competitive benefits including health coverage, financial well-being programs, and flexible time off options.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Manager for Quality Assurance on the 2nd Shift at their Devens, MA facility. The role involves leading quality oversight for cell therapy manufacturing processes, managing night-shift teams, and fostering a culture of quality and compliance.

Salary

Base: $130,020 - $157,559; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off

Skills & Requirements

Must-have

  • cGMP regulatory compliance expertise
  • Cell Therapy manufacturing process knowledge
  • Night shift leadership and management
  • Deviation and CAPA management experience
  • Cross-functional collaboration skills

Nice-to-have

  • Lean or Six Sigma improvement experience
  • Microbial controls and contamination mitigation
  • Psychological safety culture championing
  • Advanced analytical thinking abilities
  • Mentoring and staff development focus

Key Requirements

  • 8+ years of relevant cGMP experience
  • 4+ years of manufacturing site experience
  • Experience with FDA/EMA regulations in biopharmaceuticals
  • Master's degree in STEM or MBA preferred
  • Ability to work in ISO 7/8 cleanroom environments

Work Rights

Not specified

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