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.
Responsibilities
* Supporting commissioning and qualification (IQ/OQ/PQ) of high-value manufacturing equipment
* Troubleshooting automation systems and working with cross-functional teams to integrate new solutions
* Working closely with vendors during FAT/SAT, installations, and upgrades
* Contributing to the optimisation of existing manufacturing and inspection systems, including robotics and vision technologies
* Maintaining GxP documentation and ensuring compliance throughout the project lifecycle
Qualifications
* 3+ years’ experience in a GMP-regulated medical device or pharma environment
* Ideally, exposure to automation technologies (Allen Bradley, Siemens, DeltaV), robotics, or equipment validation
* Strong documentation and problem-solving skills
* Comfortable working on site with multidisciplinary teams
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