A QC Instrumentation Engineer is required to join a greenfield biotech manufacturing site in Limerick. This is a fully site based permanent position. The key focus of this role isto provide equipment lifecycle management support to the QC Laboratories. Main support functions include specifying and purchasing equipment; authoring equipment qualification packages, managing the equipment qualification process, and providing daily operational support of laboratory equipment by ensuring the equipment is maintained in a qualified state of compliance. Key Responsibilities: Author, execute, and review equipment qualification/validation protocols and strategies for the QC Laboratories. Support equipment lifecycle management and laboratory informatics initiatives. Support equipment connectivity activities, integrating QC instrumentation with LIMS and e-Systems to achieve a paper-less laboratory. Act as liaison between the maintenance team and lab personnel to schedule preventative and corrective maintenance of equipment. Responsible for coordination of laboratory CSV activities, system upgrades, and data integrity. Basic Requirements: Bachelors degree (Hons) in an engineering related field (Mechanical Engineering, Biomedical Engineering, etc.) 2 or more years of equipment experience with emphasis on GMP instrumentation. Experience supporting analytical equipment in a GMP environment. The ideal candidate will have working knowledge of CMMS, Kneat, Empower, TrackWise, LabVantage LIMS, Veeva Understanding of compliance requirements and regulatory expectations for GMP systems. For further details please contact;Paula OReillyon or send CV in confidence to Skills: Instrumentation Engineer Experience Equipment Engineering Experience GMP Experience