Job Description
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. #J-18808-Ljbffr