Job Reference: J5635387
Updated On: 19/10/2021
Status: Open to Applications
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Role OverviewWe are currently looking for a CQV Engineer to join a leading Pharmaceutical company on a 12 month contract. As the CQV Engineer, you will be responsible for working on a 200m Euro project over the next 18-24 months. Due to the urgency of this role, you must have the right to work in The Nethelands (EU citizen).
Key Duties and Responsibilities1. Working as part as a CQV team of 8-10 to deliver a project in time, on budget and safely before handing over to the client.
2. You will be responsible for delivering equipment validation and executing validation documents (IQ, OQ, PQ) within a GMP environment.
3.) Working in a large team to delivering projects in a timely manner.
Role RequirementsTo be successful in your application to this exciting opportunity as a CQV Engineer, we are looking to identify the following on your profile and past history:
1.) Relevent degree in Life Sciences or Engineering.
2.) Previous Pharmaceutical experience is essential, ideally Biotech.
3.) You must have experience in equipment validation involving generating IQ, OQ, PQ.
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