We’re hiring for a skilled Engineer to join the project team of a global medical device manufacturer in Cork. The role will support high-impact engineering initiatives tied to equipment optimisation, manufacturing automation, and the introduction of new systems on site.This is a hands-on contract position ideal for someone with strong experience in regulated environments, particularly around equipment commissioning, automated inspection systems, robotics, or vendor-based solutions.ResponsibilitiesSupporting commissioning and qualification (IQ/OQ/PQ) of high-value manufacturing equipmentTroubleshooting automation systems and working with cross-functional teams to integrate new solutionsWorking closely with vendors during FAT/SAT, installations, and upgradesContributing to the optimisation of existing manufacturing and inspection systems, including robotics and vision technologiesMaintaining GxP documentation and ensuring compliance throughout the project lifecycleQualifications3+ years’ experience in a GMP-regulated medical device or pharma environmentIdeally, exposure to automation technologies (Allen Bradley, Siemens, DeltaV), robotics, or equipment validationStrong documentation and problem-solving skillsComfortable working on site with multidisciplinary teams
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