QA/ GMP Coordinator


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Westaff is seeking experienced cGMP/ Administrative people to support the Quality Department of a well-known pharmaceutical company to prepare for regulatory audits. The position will gather documents, print and bind documents, create presentations and storyboards and do some other data input to include authoring summaries.

Requirements include: 

  • Prior experience supporting inspections
  • 2-3 years GMP documentation preferable in a pharma manufacturing company
  • Strong word, excel and powerpoint
  • Prior experience in Trackwise/ eReview or QTS is helpful


This is a very fast-paced, exciting environment offering candidates the opportunity to learn and grow!

Job Requirements

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