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QA Specialist - Document Verification

  • Location:

    Amsterdam, Netherlands

  • Contact:

    Sarah Getu

  • Job type:


  • Contact phone:

    +31 (0)20 406 97 50

  • Industry:

    Pharmaceutical , Biotechnology

  • Contact email:

Are you looking for a QA-position in the pharmaceutical biotech industry? Then this is the position for you! Apply immediately if you have experience with reviewing GMP-documentation.

Job description

You will be part of a large QA team, focus on batch records, final product labels, and logbooks. You review production and QC records, preparing them for QP release, and initiate investigations of deviations with senior QA officers. We are looking for a candidate that already has some experience with QA and GMP-Batch Record Review. If this sounds interesting, contact us immediately to discuss more details and your suitability.


  • Batch record verification
  • Final product label verification
  • Review related GMP documentation
  • Identify out of specifications and deviations
  • Initiate investigations and CAPA
  • Prepare for release by QP
  • Work under GMP guidelines


  • Bachelor's degree in a relevant field
  • At least 2 years of GMP-experience in a QA-team
  • You speak English on a professional level
  • Willing to work weekends occasionally


  • Temporary position, 1 year contract
  • Fulltime position (40 hours per week)
  • Salary range: €3500,- - €4400,- gross per month
  • Location: Amsterdam area
  • Vacancy number / Vacaturenummer; 24801