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    Associate Quality Assurance

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Associate Quality Assurance 

The company

You will be working in the European Headquarters of an American international Biopharmaceutical company. They are focusing on fighting serious, life threatening illnesses which have little to no cure. Would you like to join them on their noble mission to serve patients? 


You will provide QA guidance and support in the production area. That includes performing batch record review of batches assembled, packaged and labelled. You will have close contact with Production, Warehouse, Maintenance and Engineering, QA Management and the Qualified Person.


  • Provide daily guidance and support to Production staff

  • Act as a first point of contact in case of production queries

  • Review and approve batch production record data entries before production activities take place

  • Perform finished product checks

  • Review of operational SOP’s and Work Instructions as needed; review and approve deviation records

  • Initiate and own QA deviations as needed

  • Perform GMP compliance checks in production

  • Participate in QA production related projects as needed

  • Responsible for preparation of weekly/monthly metrics

  • Own and maintain departmental performance boards


  • University degree in Life Sciences or related field 

  • min 1-2 years of experience in a pharmaceutical company 

  • experience in batch record review and investigations is a plus

  • Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge/ experience is required 

Other information

Are you ready to take a new step in your career? If you are interested or know someone who is, contact me and upload your CV via the apply button.