We are looking for a QA Officer for a biotech firm in Hoofddorp. You review complete batch records for completeness and compliance with cGMP quality guidelines.
Job description
About 70% of your time is focused on batch record review in this role. Other duties are administration-related tasks such as archiving and preparing binders. The batch records you review are for therapies for individual patients and contain Manufacturing- and Quality Control data. You prepare the records for release by the QP and have a large responsibilities in recognizing and reporting deviations or values that are out of the specifications. We are looking for someone with some batch record review experience in a QA-department. This is a relatively junior position and candidates with a master''s degree will not be considered.
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