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CQV Engineer

  1. Midlands (Ireland)
  1. Contract
24028 (NK)
  1. Commisions, Qualification and Validation
Date Posted04 Feb 2020
Ireland is a hive of activity at present for the Life Sciences Sector with many Global Pharmaceutical / Biotechnology Organizations investing in New Facilities here.

We have an excellent opportunity for a CQV Engineer to join a global Biotech company in a state-of-the-art facility in County Westmeath initially on a 12-month contract basis.

You will be working on a clinical project and reporting into the CQV Lead.

Who are we looking for?

We are looking for an experienced CQV engineer with strong experience in the Biotech / Pharma fields.

Ideally, you will have experience with Upstream, Downstream or single use manufacturing processes

Experience working with Delta V Manufacturing Systems is also a desirable requirement and should be highlighted within your CV.

What will your role involve?

Your duties will include, but not be limited to:
  • Responsible for generating CQV test documentation which includes VQAs, VTP, DRRs and test scripts.
  • Execute testing and verification in the field on upstream and downstream processing equipment.
  • Raise and close validation deviations where required.
  • Understanding of risk-based verification approach for clean utilities, black utilities, downstream and upstream processes.
Beleive you have the right skill sets for this role? Then please apply with a copy of your CV today! 

The candidate must have the rights to work in the location stated in the job advert.

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