Lead Multiaxis CNC Lathe Programmer-Operator Reporting to the Operations Supervisor, you'll anchor our Swiss machining department at TOMZ—where precision-manufactured components for Medical Devices are produced through high-accuracy machining, finishing, assembly, and anodizing. Are you the person who… Can take a complex print, set up a Citizen or Tsugami, and be in-spec on first article? Knows when an Index multi-spindle needs a tool change versus an offset tweak? Can verify a micron-level feature on a Micro-Hite, confirm on a CMM, and document it cleanly in a QMS? Your impact You will stabilize production, elevate quality, and accelerate launches.

Picture this:

a new production order lands. You stage material, perform the setup on a Swiss lathe, apply offsets, and validate dimensions with microscopes and gauges. Mid-run, you diagnose a surface variance, correct via wear offsets, confirm on a comparator and vision system, then update the ERP and QMS so traceability is airtight. Later, you move to 3-, 4-, or 5-axis equipment—Robo Drills, mill-turn, horizontal/vertical mills—to keep delivery commitments on pace. What you'll own Setups and operation on Citizen/Tsugami Swiss lathes and Index multi-spindle lathes.

Operation across multiaxis platforms:

Robo Drills, mill-turn systems, and horizontal/vertical mills. Tool changes, offsets, and cycle optimization with minimal support. Visual/dimensional inspection using microscopes, micrometers, calipers, pin/thread gauges, comparators, Micro-Hite, CMM, and vision systems.

ISO 13485

documentation; ERP/QMS entries for inspection and full traceability. Material control, identification, and traceability for conforming and nonconforming product. Preventive maintenance and first-response troubleshooting of complex machine/process issues. Quality Best Practices and continuous improvement in GDP/GMP; mentoring and training of lower-level machinists. Enable a culture focused on quality and delivery; follow safety and PPE requirements; adhere to the TOMZ Quality Management System. Perform other duties as assigned in support of production goals. What we value Experience producing Class I, II, and/or III medical device components within a regulated environment using calibrated equipment and hazardous materials. Transferable manufacturing experience from aerospace, defense, or automotive. GMP/ISO knowledge and

ISO 13485

familiarity; strong grasp of machine usage, care, and inspection processes. Blueprint/spec reading skills; intermediate GD&T competency. Hands-on capability with hand tools for PM, repairs, and tool changes. Meticulous, organized approach with an eye for nonconformances. Self-starter who thrives independently and within cross-functional teams (R&D, Manufacturing, QA); strong verbal and written English communication. Education and experience 3-7 years of experience in a regulated manufacturing environment. Technical school certification or equivalent, directly transferable experience in manufacturing/engineering; certification strongly preferred. Physical and safety considerations Ability to sit or stand for prolonged periods. PPE may be required, including dust masks, ear plugs, and cut-resistant or chemical-resistant gloves; engineering controls may be used.