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QA Specialist - GMP

  • Location:

    Amsterdam, Netherlands

  • Contact:

    Natanael Hazel

  • Job type:

    Temp to Perm

  • Contact phone:

    +31 (0)20 406 97 50

  • Industry:

    Life Sciences, Biotechnology

  • Contact email:

    natanael_hazel@oxfordcorp.com

Do you have a few years of experience as QA Officer and are you looking for a next challenge? Then this position as QA Specialist might be a perfect fit for you! Apply below or reach out to one of our science recruiters!

Job description

As QA-Specialist, you are able to review a wide range of GMP documentation independently. You do work in a motivated an international team of QA professionals, but have sufficient experience to review batch records, QC data, and oversee investigations and CAPAs. This position is mainly office-based, but you will occasionally be on the floor to help with process improvements and investigations.
Overall, you have a broad role in quality and assure that this pharmaceutical company can produce safe medication.

Responsibilities

  • Review of GMP documentation;
  • Batch record review
  • Investigations
  • CAPAs
  • QC data
  • Process improvement


Desired Profile

  • Bachelor's degree in any relevant field
  • Demonstrable QA experience under GMP or extensive documentation experience in QC
  • Good knowledge of quality and compliance
  • Full working proficiency English, Dutch is a plus
  • You hold a work permit for The Netherlands, visa sponsorship is not possible


Benefits

  • Long term position - initial contract 1 year
  • Salary range: €4000 - 5500
  • Fulltime position, 32h is possible
  • Region: Amsterdam, some remote work is possible (1-2 days per week)

Vacancy number: 22239