Validation Engineer - West of Ireland
DPS now require a Validation Engineer for a large Pharmaceuticals manufacturing organisation in the greater Mayo area. This role will be specifically charged with coordinating and executing the validation documentation for predetermined laboratory equipment.
Responsibilities:
* Generation and execution of validation lifecycle documentation (IQ,OQ,PQ).
* Sourcing & purchasing of reliable laboratory equipment.
* Review of vendor prepared/executed commissioning & validation documentation.
* Reporting of Validation non-conformances and providing solutions to remediate issues.
* Working with cross function departments to ensure solutions are implemented in an efficient and effective manner.
* Review of the impact of change on the maintenance of the validated state, including execution of re-validation as required.
* Processing documentation through the document management system.
* Periodic review of documentation management system workflows to ensure both regulatory & business needs are satisfied.
Requirements:
* Qualification and/or degree in engineering or scientific discipline.
* 3 years + validation experience in a GMP environment.
* Should have a track record of carrying out and executing GMP/FDA documentation.
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