As the new QA Officer you'll be working at a dynamic, globally active company.


We offer you exciting work as part of a team of experts who treat each other as equals. All over the world. In our biopharmaceutical organization with sites in Germany and the Netherlands we are fast-growing. At our Amsterdam-based center the focus lies on the GMP-compliant microbial based production of recombinant proteins, vaccines and live microbials as drug substance and drug product.

Your tasks will be:

  • Writing and review of GMP documents Writing and review of deviations, CAPAs, environmental and utility monitoring system investigations and reports, change controls
  • Participate in project teams as MF project lead
  • Execution of internal audits according to audit plan and support during external audits (clients and governmental bodies)
  • Coordination, maintenance and administration of manufacturing systems.
  • Training Coordinator Chairman of Tier meetings and environmental and utility monitoring board Meetings
  • Profound knowledge of Dutch and English language, verbally and written

Functie eisen

  • Minimum of education of HBO level in the orientation of Chemistry, (Micro)Biology or Pharmaceutical Sciences
  • A minimum of 4 years experience in the pharmaceutical industry
  • A few years experience as a QA Officer
  • Excellent verbal and written communication skills
  • Ability to work with tight deadlines and handle multiple tasks
  • Computer fluency in MS Office, e.g. Word, Excel, PowerPoint; knowledge of TrackWise is a plus
  • Experience with FDA compliance is a plus


Exciting work as part of a team of experts who treat each other as equals. All over the world.

Sollicitatie Procedure

Contactpersoon voor deze functie is Diederik van Straalen, bereikbaar op telefoonnummer 023 55 78 529 of via e-mail: Kenmerk: 8604.

Solliciteer nu
  • Functienaam:
    QA Officer
  • Locatie:
  • Branches:
  • Opleidingsniveau:


Vacature: QA Officer

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