Senior CMM Programmer

Torrey Holistics; Berlin (CT); On-site; USD 85,000 - 120,000; Full time

Job summary

TOMZ seeks a metrology-focused engineer to advance measurement methods in a regulated medical device setting. You will program CMMs and vision systems, develop robust test methods, and collaborate across departments to ensure compliant inspection plans and data-driven quality decisions.

Contribute to calibration, CAPA, and QA activities while supporting incoming, in-process, and final inspections; travel up to 5% annually may be required.

Qualifications

• 4+ years in a regulated manufacturing environment.
• 3+ years in manufacturing quality with advanced metrology including CMM and/or vision systems.
• 3+ years of GD&T and measurement programming system training.

Responsibilities

• Develop advanced metrology approaches for medical device manufacturing and document control.
• Program and operate measurement platforms: vision systems, CMMs, PLCs, optical comparators and sensors, laser systems.
• Lead First Article Inspections (FAIs) and support gage calibration review and calibration standards.

Skills

GD&T

Metrology

CMM programming

Vision programming

Gage calibration

Regulatory knowledge

Education

High School Diploma or GED

ASQ-CQT/CQE/CRE

DMIS certification

Tools

CMM software

Vision system software

PLC systems

Job description

Step into a day where precision drives patient outcomesYou arrive at TOMZ, open the latest print, and translate complex GD&T into a confident inspection plan. Before first shift finishes their coffee, you have a CMM program verifying a critical implant feature and a vision system queued for incoming components. By lunch, you have tuned a laser measurement routine, advised production on a new test method, and coached a teammate through a tricky bench layout. It is all part of advancing metrology in a regulated medical device environment—and it is exactly where you thrive.What you will ownDevelop advanced metrology approaches for medical device manufacturing, assessing process risk and implementing effective controls, corrective and preventive actions, and refined test methods.Operate and program measurement platforms: vision systems, CMMs, PLCs, optical comparators and sensors, and laser measurement systems.Serve as the GD&T subject matter expert; translate complex tolerances into practical inspection strategies and bench/surface plate layouts.Collaborate to define and document test methods; execute and evaluate Test Method Validations.Apply precision tools expertly: electronic height gages, calipers, micrometers, depth gages, indicators, and plug/thread Go/No-Go gages.Design, model, and build inspection workholding and custom fixtures.Provide hands-on leadership for Incoming, In-Process, and Final inspection plans; champion First Article Inspections (FAIs).Support gage calibration review, management, execution, and evaluation; establish and uphold calibration standards.Contribute to materials testing (chemistry and mechanical) when needed.Promote Quality Best Practices and GDP/GMP continuous improvement across the organization.Track and report inspection data: rejection rates, defect modes, and process trends across customers and product families.Review ECOs for releasing Quality Engineering documentation; create clear inspection instructions.Adhere to the TOMZ Quality Management System and perform other duties as assigned.What you bringSelf-starter who excels in a fast-paced setting; strong English verbal/written communication.Microsoft Office proficiency and a basic grounding in statistics and sampling strategies.4+ years in a regulated manufacturing environment.3+ years in manufacturing quality with advanced metrology, including CMM and/or vision system programming.3+ years of GD&T and measurement programming system training.Education: High School Diploma or GED.PreferredASQ-CQT, CQE, or CRE; DMIS programming certifications.Class I, II, and/or III medical device experience; experience in regulated industries such as aerospace, defense, or pharma.Familiarity with ISO 9001, ISO 13485, 21 CFR 820, and EU MDR, including design controls, GMP, supplier qualification, auditing, quality control (GD&T, Nonconforming Materials, MRB), CAPA, and customer complaint handling.TravelUp to 5% annually; may include multiple overnights and occasional weekends.Physical requirements and work environmentAbility to bend, stoop, squat, kneel, and lift up to 30 pounds; team lift or mechanical assist required for heavier objects.Exposure to oil, grease, occupational noise, cleaning solvents, dust, metal particles, sparks, coolant, and sharp-edged materials; PPE such as safety glasses, dust masks, ear plugs, cut-resistant or chemical-resistant gloves, and engineering controls may be required.Ability to sit for extended periods; proficient keyboard/mouse use; sustained computer and visual work with correction as needed; repetitive hand/arm motions.