Job Title: Quality Inspector/CMM Programmer Department: Quality / Operations Reports To: Quality Manager Role Purpose To ensure all manufactured and purchased components meet specification and regulatory requirements through effective visual, dimensional, and CMM inspection, supporting compliant product release in a high-precision, regulated orthopaedic manufacturing environment.Like the look of this opportunity Make sure to apply fast, as a high volume of applications is expected Scroll down to read the complete job description.This will progress to an evening shift role to support production.Key Responsibilities Perform visual and dimensional inspection of metal and plastic components to drawings and specifications Create, execute, and maintain inspection plans, sampling plans, and control documentation Interpret engineering drawings and GD&T requirements accurately Program and operate CMM equipment / Vision Systems for routine and complex measurements
- Develop, validate, and maintain CMM programs Perform in-process, first article, and final inspections Complete FAIRs / ISIR / PPAP documentation where required Ensure traceability, documentation accuracy, and compliance with ISO 13485 / FDA regulations Support non-conformance investigations, root cause analysis, and corrective actions Work closely with Manufacturing, Engineering, and Quality teams to resolve quality issues Maintain a clean, controlled inspection environment Support continuous improvement initiatives in inspection methods and process capability Skills & Experience Required Proven experience as a Quality Inspector/Technician in precision manufacturing (medical device or orthopaedics preferred) Strong experience in visual inspection of aesthetic and functional surfaces Advanced ability to perform dimensional inspection with manual tools and advanced equipment Strong experience reading engineering drawings and GD&T Experience programming and running CMM machines (PC-DMIS / Zeiss Calypso / Mitutoyo / Microview or equivalent) Working knowledge of ISO 13485 / FDA 21 CFR 820 Strong attention to detail and documentation discipline Excellent problem-solving mindset Comfortable working in a regulated, audit-ready environment Desirable / Advantageous Experience in orthopaedic implants or medical manufacturing Knowledge of surface finish standards, polishing inspection, burr/edge inspection SPC, MSA, Gage R&R experience Experience with laser scanners, optical comparators, vision systems Diploma / Degree in Mechanical, Manufacturing, Production, Quality Engineering.Personal Attributes Highly detail-oriented and methodical Strong communicator and team collaborator Quality-driven mindset Ownership and accountability What We Offer Competitive salary and benefits package
- €40k
- 45k basic, Health Care, pension contributions, shift allowance 25% Opportunities for training and development Modern equipment and a forward-thinking manufacturing environment Career progression in a growing team KSGalway Should you require any support or assistance, please contact your local Gi Group office.Gi Group Holdings Recruitment Limited are proud founding members of Menopause in business, pledge members for Neurodiversity in business, Disability committed members, Gold status pledge members for the Armed Forces Covenant, and Bronze trail blazers for Racial Equality matters.Gi Group Holdings Recruitment Limited group of companies includes Gi Recruitment Limited, Draefern Limited, Gi Group Recruitment Ltd, INTOO (UK) Limited, Marks Sattin (UK) Limited, TACK TMI UK Limited, Grafton Professional Staffing Limited, Encore Personnel Services, Gi Group Ireland Limited and Kelly Services (UK) Ltd.Gi Group Ireland Limited are acting as an Employment Agency in relation to this role.We are committed to protecting the privacy of all our candidates and clients.If you choose to apply, your information will be processed in accordance with the Gi Group Privacy Statement.
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