Head Of Qa Technical Operations

Bristol Myers Squibb

Summit, NJ, United States
Base: $223,640 - $270,993; bonus/equity: + incenti...
50% onsite
Cgmp operations oversight
Quality technical operations leadership
Investigations, capa, change controls
Responsible for leading the day-to-day quality review and approval of investigations, CAPA, Change Controls with associated documents and the oversight of the Quality Engineering team responsible for qualifications and validations

Job Summary

  • Responsible for leading the day-to-day quality review and approval of investigations, CAPA, Change Controls with associated documents and the oversight of the Quality Engineering team responsible for qualifications and validations.
  • Drives for operational adherence to applicable cGMP regulations, BMS policies and procedures, and provides direction to Operations, Facilities, QC, and QA teams for planned and unplanned deviations.
  • 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

Responsible for leading the day-to-day quality review and approval of investigations, CAPA, Change Controls with associated documents and the oversight of the Quality Engineering team responsible for qualifications and validations.

Salary

Base: $223,640 - $270,993; 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

  • cGMP operations oversight
  • Quality Technical Operations leadership
  • investigations, CAPA, Change Controls
  • qualification and validation oversight
  • GMP operations audits and inspections

Nice-to-have

  • strategic transformational programs
  • fosters rich team culture
  • high business acumen
  • embraces complexity strives for simplicity

Key Requirements

  • Bachelor's degree in Science or Engineering
  • 15+ years of experience in Quality Assurance
  • 7 years of people management experience
  • Expertise in GMP for Pharmaceutical/Biotech/ATMP Manufacturing
  • Experience with clinical and commercial product manufacturing

Work Rights

Not specified

Tailored Resume

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