QC Inspector

Job Title: QC Inspector Locations: Burlington, MA Duration: 03+ Months The ideal profile would include: 5+ years of mechanical inspection experience GD&T experience Engineering drawing interpretation CMM knowledge (Zeiss Calypso, PC-DMIS preferred) Vision systems experience (Keyence preferred) Candidates with strong mechanical inspection backgrounds who can hit the ground running with minimal training will be considered. Responsibilities Receiving Inspection: QSR support such as calibration, product testing, label control, etc. Receiving inspection of components following procedures, specifications, and drawings. Utilize a variety of standard metrology equipment, including optical comparator, height gauge, master height gauge, Zeiss CMM, Keyence Vision Metrology System, calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. Read engineering drawings and interpret geometric dimensioning and tolerancing. Review associated paperwork, complete inspection records using good documentation practices, and release components. Program the Zeiss CMM and Keyence VMS to run automatic routines for multiple part inspections. Inspection of machined and injection molded components, PCBs, off the shelf components, etc. In-Process Inspection: Perform line clearance for operations activities. Inspect and release labeling. Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. Perform inspections and testing on components and assemblies in manufacturing. Final Inspection: Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. Perform final inspection and test on finished goods. Other Duties: Work with engineering in the design of high-quality inspection/metrology fixtures. Support equipment and process validation activities by inspecting process outputs. Execute Gage R&R activities. Ensure daily quality records and company practices are compliant with internal procedures and quality system requirements. Other projects as requested by supervisor. Experience Level 2: 3-7 years industry experience Level 3: 7-10 years industry experience Medical device experience and working knowledge of QSR a must Experience working in a fast‑paced electro‑mechanical environment. Attention to detail and accuracy a must Must have excellent documentation skills Team player, good written/oral communicator Education College courses or degree preferred #J-18808-Ljbffr Creative Solutions Services, LLC