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QA Batch Record

QA Batch Record

LocationLeiden, Netherlands
Business SectorBiotechnology
Contact nameMerel van Os
Contact emailm.vanos@panda-int.com
Job ref21342
Published3 months ago

The QA contractor acts as a quality expert and applies our Quality Systems to create, review and approve GMP documentation. The contractor works in close collaboration with other departments. First assignment 6 months, Leiden (high chance of extension).



  • Activities include, but are not limited to:
  • Paper and electronic batch record review
  • Raw material release
  • Document revisions review and approval
  • Review and approve analytical method transfer protocols and reports
  • Review and approve change controls, validation protocols and reports, validation assessments, and applicable lifecycle documentation depending on experience.
  • Track and monitor the progress of changes to anticipate, flag, and prevent any delays in change implementation.
  • Depending on experience supporting master material changes



  • BSc/HBO (or equivalent) in bioscience, chemistry, pharmacy or equivalent;
  • +1 year of QA experience in pharmaceutical or related industry;
  • Up-to-date knowledge of current GMP regulations;
  • Experience in Change control and all documenting related activities;
  • Experience with documentation systems like Trackwise, True Vault is preferable;
  • Good communicative and advisory skills in both Dutch and English, both (verbal and written);
  • Able to work independently as well as in a team.



If you are interested in the above description, please apply today. The job interview and offer can take place within the next 2 weeks. For more information, you can contact Merel van Os at +31 (0)20 20 44 502 or via email at m.vanos@panda-int.com.