Quality Control Inspector II

Job Title: QC Inspector II Location: Burlington MA Shift: Mon thru Fri (40 hours) Duration: Est 6 months Description: Overview: Responsibilities include all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, product testing, label control, etc. Daily Functions: Receiving Inspection 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 good 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. Ensures daily quality records and company practices are compliant with internal procedures and Quality System requirements. Other projects as requested by supervisor. Work Experience Level 2: 3-7 years industry experience Medical device experience and working knowledge of QSR a must Experience working in a fast-paced electro-mechanical environment. ttention to detail and accuracy a must Must have excellent documentation skills Team player, good written/oral communication Education High School Diploma with work exp. College courses or degree preferred

Created: 2026-03-04