Senior CMM Programmer

Do you see tolerance stacks as a roadmap? Ready to turn them into reality?Join TOMZ and lead the dimensional assurance that keeps our medical devices trusted in the field. Imagine partnering with manufacturing in the morning to de-risk a new process, then rolling up your sleeves in the afternoon to build a fixture and validate a test method—closing the loop with actionable data that sharpens quality across product families.You willAdvance metrology strategies for medical device manufacturing by evaluating process risks, implementing controls/CAPA, and developing robust test methods.Program and run vision systems, CMMs, PLCs, optical comparators/sensors, and laser measurement systems.Act as the GD&T SME and bench layout expert to solve complex measurement problems.Co-create clear test methods and carry out Test Method Validations with thorough evaluation.Leverage precision instruments: electronic height gages, calipers, micrometers, depth gages, indicators, and plug/thread Go/No-Go gages.Design/model/build inspection workholding and specialized fixtures.Guide Incoming, In-Process, and Final inspection plan execution; own First Article Inspections.Manage gage calibration activities end-to-end and define calibration standards.Contribute to materials testing in chemistry and mechanics as required.Drive Quality Best Practices and GDP/GMP continuous improvement initiatives.Analyze and report inspection data, highlighting rejection rates, defect signatures, and trends by customer/product family.Review ECOs to release Quality Engineering documentation; produce precise inspection instructions.Follow the TOMZ Quality Management System and perform other duties as assigned.You bringProactive, fast-paced work style; clear English communication in writing and speech.Comfort with Microsoft Office and foundational statistics/sampling.4+ years in a regulated manufacturing environment.3+ years in manufacturing quality with advanced metrology, including CMM and/or vision programming.3+ years of GD&T and measurement programming system training.High School Diploma or GED.Bonus pointsASQ-CQT, CQE, or CRE; DMIS programming certifications.Background in Class I/II/III medical devices and/or aerospace, defense, or pharmaceutical sectors.Hands-on familiarity with ISO 9001, ISO 13485, 21 CFR 820, and EU MDR, plus design controls, GMP, supplier qualification, auditing, QC (GD&T, Nonconforming Materials, MRB), CAPA, and complaint handling.TravelApproximately 5% annually; may require multiple overnight trips and occasional weekends.Physical realities of the roleAbility to bend, stoop, squat, kneel, and lift up to 30 lbs; team lift/mechanical assist above 30 lbs.Regular exposure to oil, grease, noise, cleaning solvents, dust, metal particles, sparks, coolant, and sharp-edged materials; PPE and engineering controls may be required (safety glasses, dust masks, ear plugs, cut-resistant or chemical-resistant gloves).Prolonged sitting with extensive keyboard/mouse use; sustained visual focus with correction if needed; repetitive hand and arm movements. #J-18808-Ljbffr