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QA Manager - GMP Manufacturing

As QA Manager, you are responsible for the QA officers on all levels. You oversee all quality aspects of the GMP manufacturing and QC testing.

Job description

You manage a relatively large team (~12 FTE) of QA staff and ensure that the entire Manufacturing process is executed under GMP compliance. You are responsible for the batch record review, release, timely action on deviations, investigations, and CAPAs. You are frequently in contact with clients and play an important role in audits. Complicated quality matters are occasionally escalated to you, but the main focus is overseeing and supervising the team.

Responsibilities

  • Supervise QA staff (!12 FTE)
  • Oversee Manufacturing quality
  • Ensure GMP compliance
  • Participate in complex CAPAs, investigations and deviations
  • Facilitate personal and professional growth of your team


Requirements

  • BSc degree (or higher) in any relevant field
  • Elaborate quality experience in the pharmaceutical industry (8+ years)
  • Management experience (5+ years)
  • Fluent in English, Dutch is a plus
  • (Unlimited) EU work permit


Benefits

  • Contract: direct contract for a year, permanent extension is realistic
  • Salary indication: €6000 - €8000 depending on experience
  • Working hours: office hours, fulltime, 4 days possible
  • Location: Amsterdam

Vacancy number: 21780