Senior Specialist, Qa Operations Investigations

Bristol Myers Squibb

Leiden, Netherlands
50% onsite
Quality review and approval
Manufacturing and laboratory investigations
Cgmp compliance
The Senior Specialist, QA Operations Investigations is responsible for the quality review and approval of manufacturing and laboratory investigations at the CTF in Leiden, ensuring compliance with global current Good Manufacturing Practice (cGMP)

Job Summary

  • The Senior Specialist, QA Operations Investigations is responsible for the quality review and approval of manufacturing and laboratory investigations at the CTF in Leiden, ensuring compliance with global current Good Manufacturing Practice (cGMP).
  • Duties include reviewing and approving investigations, CAPAs, and effectiveness checks, potentially authoring technical reports, and ensuring CAPAs adequately address root causes.
  • Bristol Myers Squibb offers a work environment that values balance and flexibility, with competitive benefits and opportunities for growth in a role that transforms patient lives.

Matching Summary

The Senior Specialist, QA Operations Investigations is responsible for the quality review and approval of manufacturing and laboratory investigations at the CTF in Leiden, ensuring compliance with global current Good Manufacturing Practice (cGMP).

Skills & Requirements

Must-have

  • Quality review and approval
  • Manufacturing and laboratory investigations
  • cGMP compliance
  • CAPA effectiveness checks
  • Root cause analysis tools

Nice-to-have

  • Continuous improvement goals
  • Cross-functional collaboration
  • Innovative solutions
  • Positive team environment

Key Requirements

  • 4+ years regulated industry experience
  • 1+ year deviation experience
  • Bachelor's degree preferred
  • Experience with electronic systems and databases
  • Experience with root cause analysis tools

Work Rights

Not specified

Tailored Resume

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