DPS are currently seeking a number of CQV resources to work on an expansion project for our client who are a global Pharmaceutical company. The contract will be based in Wrexham
* Strong experience in the biopharmaceutical or pharmaceutical industry (Validation, Technical Services or Quality).
* Direct experience in cGMP validation activities
* Extensive knowledge of Validation regulations, current industry practices, and experience of interpretation and application of guidelines and regulations
* Excellent technical writing skills
If you would be interested in discussing this opportunity in more detail, please send through your updated CV
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