Cork city, Ireland | Posted on 02/20/2026Industry Pharma/Biotech/Clinical ResearchCity Cork cityState/Province CorkCountry IrelandJob DescriptionAbout PSC BiotechWho are we?PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.‘Take your Career to a new Level’PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.Employee Value PropositionEmployees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.Overview:We are seeking a motivated QC Equipment Specialist in Cork! To join a dynamic QC team, supporting the calibration, maintenance, and qualification of laboratory equipment in a regulated environment. This role offers hands-on experience with GMP/GxP practices, vendor management, and quality documentation perfect for candidates looking to grow their career in QC and laboratory support.RequirementsResponsibilities:Coordinate the calibration, maintenance and repair of analytical laboratory instruments and support equipment using the Enterprise Computerized Maintenance Management System (CMMS).Responsible for the completion of QC equipment related documentationsPerform change request using the Enterprise Quality Management System (Trackwise)Maintain good working relationships with vendors to ensure vendor meets current and future needsWork with vendors to troubleshoot equipmentMaintain the laboratory equipment inventory for tracking equipment assets and vendor contactsMaintain the electronic and paper inventory for equipment qualification packagesPerform equipment inventory reconciliation with physical assets in each laboratory; assessing the current and future suitabilitySkills:0-3 years of experience working in a GMP environmentSome experience in quality control practices, current Good Manufacturing Practices or Good Laboratory PracticesUnderstanding of GxP guidelinesMust have excellent record keeping, written and verbal skillsAbility to perform most tasks with minimal supervisionComputer literacy is requiredExperience with Microsoft Excel and Word is requiredEducation:BS/BA in Life Sciences or equivalent experience
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