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Cleaning Validation Engineer

  1. West
  1. Contract
  1. Commisions, Qualification and Validation
Date Posted25 Oct 2019
Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing manufacturing facilities all over the country. An exciting opportunity has arisen to work via Quanta on the client’s side for a global Pharmaceutical organisation on an expansion project based in the picturesque Munster region of Ireland.

Located just 20 minutes from the nearest international airport, the manufacturing site is workable for those wishing to commute to/from Ireland for a contract position. You will be required on site for 5 days per week Monday – Friday working 45 hours.

We have multiple requirements at present in the Cleaning Validation and SIP remits for both Executor / Engineer level and Technical Writer positions to support these teams. If you have experience with Cleaning Biopharmaceutical Equipment, SIP (Steam in place) equipment or writing technical documents for cleaning validation teams, then please send in your CV for review!

The ideal candidate will have the following experience:
  • Pharmaceutical Industry experience is a must
  • Experienced in QA Validation activities
  • Execution of cleaning validation protocols.
  • Experience on writing and approving Deviations/ GMP documents
  • Execution, review & approval of SIP/ CIP and continuing validation protocols and closure
  • Extensive experience on writing and approving Deviations
  • Technical writing experience has written a number of white papers and site reports.
  • Technical writing experience for continuing validation assessments
If this role seems of interest to you, please get in touch to find out more.

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