OverviewValidation Engineer (Cleaning) - Ireland, Cork - 12 Months Initial ContractOur client is undergoing major growth, supported by substantial investment aimed at increasing its overall manufacturing capacity in the medical device sector. Recent upgrades include the development of new, advanced automation systems and additional infrastructure enhancements designed to meet growing global healthcare demands. With a long established presence and a highly skilled workforce, the site requires the role of a Validation Engineer to join their project based in Cork.What you’ll doSupport and execute validation activities for pharmaceutical manufacturing equipmentCarry out thermal validation studies on: Autoclaves, SIP (Sterilisation-in-Place) systems and Temperature-controlled unitsPerform cleaning validation for tanks, process lines, and equipment partsGenerate, review, and approve validation documentation (Validation Plans, IQ, OQ, PQ)Work closely with internal teams and external vendors to: Develop User Requirement Specifications (URS), Support Factory Acceptance Testing (FAT) and Ensure Quality by Design (QbD) principles are followed.What you’ll needExtensive experience in pharma/biopharma industryMinimum bachelor’s degree in engineeringStrong knowledge of: GMP (Good Manufacturing Practice), Validation lifecycle (IQ/OQ/PQ), Cleaning and thermal validation principlesIf this role is of interest, apply now!#LI-KC1
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