Associate Director, Qc Technical Services

Bristol Myers Squibb

Summit West, NJ, US
Base: $163,850 - $198,543; bonus/equity: + incenti...
Hybrid (50% onsite)
Expert cgmp quality systems knowledge
Root cause analysis and capa implementation
Internal qc audit program development
Bristol Myers Squibb is seeking an Associate Director for Quality Control Technical Services to oversee compliance, investigations, and quality metrics while managing a team in Summit West, NJ. The ideal candidate should possess extensive cGMP knowledge and leadership experience, with a focus on quality systems and process improvements

Job Summary

  • This role is responsible for overseeing the Quality Control Compliance organization, including investigations, deviations, and change controls.
  • The position requires coordinating internal and external audits while ensuring alignment with global cGMP policies and standards.
  • Bristol Myers Squibb offers a competitive compensation range of $163,850 to $198,543 along with comprehensive health and wellbeing benefits.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director for Quality Control Technical Services to oversee compliance, investigations, and quality metrics while managing a team in Summit West, NJ. The ideal candidate should possess extensive cGMP knowledge and leadership experience, with a focus on quality systems and process improvements.

Salary

Base: $163,850 - $198,543; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • Expert cGMP Quality Systems knowledge
  • Root cause analysis and CAPA implementation
  • Internal QC audit program development
  • Cross-functional stakeholder collaboration
  • Health authority inspection support

Nice-to-have

  • Industry benchmarking experience
  • Employee development and mentoring skills
  • High-level data communication abilities
  • Strategic quality initiative conceptualization

Key Requirements

  • 7-10 years relevant cGMP Quality work experience
  • Minimum 5 years of leadership experience
  • University degree required
  • Proven track record in root cause analysis

Work Rights

Not specified

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