Junior Precision Manufacturing Machinist — ISO 13485 Environment

Junior Precision Manufacturing Machinist — ISO 13485 Environment

Do you enjoy bringing tight-tolerance parts to life on multiaxis CNC equipment?

Want to start or grow your career building components for medical devices in a regulated setting?

At TOMZ, you will report to the Operations Supervisor and help turn engineered drawings into inspected, traceable parts.

Imagine this

You load material, verify setup, and run a first article on a Citizen or Tsugami Swiss lathe.

The comparator and Micro-Hite confirm dimensions, and you record results in our ERP and QMS.

Mid-shift, a mill-turn presents a complex alarm—working with your team, you diagnose tooling wear, adjust offsets, and resume production.

Before you clock out, you complete inspection documentation and confirm material status and traceability.

• In this role, you will
• Operate and maintain 3-, 4-, and 5-axis equipment: Robo Drills, mill-turns, horizontal/vertical mills, CNC Swiss (Citizen, Tsugami), and Index multi-spindle lathes.
• Conduct visual and dimensional inspections using a microscope, micrometers, calipers, pin/thread gauges, comparator, and Micro-Hite.
• Document to ISO 13485 standards, compiling quality inspection records and maintaining material identification and traceability for conforming and nonconforming product.
• Use ERP and QMS tools to control inspection records and product status.
• Support root-cause and problem-solving efforts for challenging machine or process issues.
• Follow the TOMZ Quality Management System, maintain safe conditions, wear required PPE, and perform other duties as assigned.
• Contribute to Quality Best Practices and continuous improvement of GDP/GMP.

What you bring

• Basic understanding of machining equipment operation, care, and inspection methods.
• Ability to use hand tools for preventive maintenance, repairs, and tool changes.
• Competence reading blueprints, specifications, and procedures.
• Detail orientation and the ability to complete work accurately and promptly.
• Foundational GD&T and familiarity with GMP/ISO.

Experience baseline

• 0-2 years in a regulated manufacturing environment.
• Bonus experience
• Class I, II, and/or III medical device manufacturing exposure.
• Time in regulated sectors such as aerospace, defense, or pharmaceutical.
• Strong English communication skills, written and verbal.
• Physical demands
• Bend, stoop, squat, kneel, and lift up to 50 pounds; team lift or mechanical assist required over 50 pounds.
• Repetitive hand and arm movements while handling up to 20 pounds; grip, twist, and place components for extended periods; lift overhead.
• 20/20 vision (assisted or unassisted) for sorting raw and non-conforming materials; good dexterity for small-to-medium products.
• Work around oil, grease, occupational noise, cleaning solvents, dust, metal particles, sparks, and coolant; PPE such as safety glasses, dust masks, ear plugs, and cut-resistant or chemical-resistant gloves, plus engineering controls, may be required.
• Ability to sit or stand for extended periods.
• Tools you will touch
• CNC Swiss lathes (Citizen, Tsugami), Robo Drills, Index multi-spindle lathes, horizontal and vertical mills, and precision measurement tools including comparator and Micro-Hite.