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Validation Engineer - Laboratory Equipment/Systems - GMP

  1. West
  1. Contract
  1. Commisions, Qualification and Validation
Date Posted06 Mar 2020
Newly built Biopharmaceutical manufacturing facility has a contract requirement for an experienced
Lab Validation Engineer to generate, review & approve the IOPQ protocols and validation documents for the Laboratory Systems & Equipment.

Manufacturer of Sterile liquid injectibles we are looking for an experienced Validation Engineer who has previous experience of Laboratory Equipment & systems qualification experience within a GMP environment  to carry out the following:

  • Oversee the execution activities on the Laboratory Systems and related operational software packages
  • Generate/Review & Approve Validation documents related to Laboratory,  IT Infrastructure  IT/ Lab/ Enterprise projects currently being introduced on site.
  • Implement the qualification program for the qualification of laboratory and/or manufacturing equipment which will include:
  • Equipment Qualification Assessments
  • Installation Qualifications (IQs), Operational Qualifications (OQs), and where applicable Performance Qualifications (PQs)
  • Execution for IQ, OQ and PQ

Call me for further information on this vacancy! 

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

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