Galway – This is your chance to gain invaluable experience within one of the biggest medical technology companies in Ireland! You will have the opportunity to progress internally, working with some of the best engineers in Europe, solving and innovating as you go! Job Overview: Control of Non-Conforming Product and Reporting of Non-Conforming Events Compiling Non Conformance Review Board Reports each month. Compiling various documents for Management on an ad hoc basis Responsibilities: Ensure compliance to applicable regulatory standards and current GMP procedures and practices. Control of non-conforming product and documentation of non-conforming Events. Perform product defect analysis. Routine verification of product release criteria and recording of test results. Support Core Team Problem solving activities. Update QA documentation Management of product reworks as required, with direction from Quality and Manufacturing Engineer. Control of non-human use build components… – Permanent – Full-timeApply for this job.