Swiss Machinist – II

Summary of Position

Reporting to the Operations Supervisor, this position will have direct responsibility for the set-up and manufacture of components within a machining Department. TOMZ manufactures parts via high- precision metal machining, finishing, assembly, and anodizing processes for Medical Devices. The successful candidate will be expected to maintain the ISO 13485 standards documentation, set up and operate equipment, and perform visual and dimensional inspections on machined components using various precision measuring equipment.

Essential Functions

• Set up and operate and maintain Citizen Lathes or Tsugami Lathes
• Perform offsets and tool changes to ensure efficient production with minimal support.
• Set up legacy components and new production orders for steady machine operation.
• Perform preventative maintenance on Swiss Lathe to ensure consistent machine performance
• Conduct visual and dimensional inspections using microscopes, micrometers, calipers, pin gauges, thread gauges, comparators, Micro-Hite, CMM, and vision systems.
• Perform scheduled and regular preventive maintenance on equipment.
• Drive problem-solving activities for complex machine or process issues.
• Complete and compile documentation related to quality inspection standards.
• Ensure proper material control, identification, and traceability for conforming and nonconforming materials.
• Support Quality Best Practices and contribute to continuous improvement in GDP/GMP.
• Utilize ERP and QMS systems to document and control inspection and traceability activities.
• Maintain safe working conditions and follow occupational safety and health requirements, including PPE guidance.
• Adhere to the TOMZ Quality Management System.
• Perform other duties as assigned.

Qualifications:

Education

• High school diploma, GED, or equivalent directly transferrable work experience (Manufacturing or Engineering discipline preferred).
• Certification from a technical school program preferred.

Experience

• Minimum of 2-5 years’ experience in a regulated manufacturing environment.

Qualifications

• Experience in Class I, II, and/or III medical device manufacturing within a regulated environment using calibrated equipment and hazardous materials.
• Strong math background, preferable in machine math/shop math
• Relevant job experience in regulated manufacturing, with industry experience in aerospace, defense, or automotive.
• Knowledge of and experience with GMP/ISO standards.
• A self-starter capable of working independently and as part of a team, with the ability to collaborate across various functional areas, including R&D, Manufacturing, and QA, to achieve results with guidance.
• Understanding of mechanical equipment usage, care, and inspection processes.
• Ability to use hand-held tools for preventive maintenance, repairs, and tool changes.
• Effectively read and understand blueprints, specifications and procedures.
• Understanding of GD&T.
• Detail-oriented with the ability to maintain accuracy and complete tasks promptly.
• Identify nonconformances and maintain organization.

Preferred Skills

• Strong verbal and written English language communication skills.

Physical Demands

• Ability to bend, stoop, squat, kneel, and lift up to 50 pounds. Team lift or mechanical assistance required for objects over 50 pounds.
• Perform repetitive hand and arm movements while lifting up to 20 pounds, including gripping, twisting, and placing components for extended periods, and lifting objects overhead.
• 20/20 vision (assisted or unassisted) required for sorting raw and non-conforming materials. Good dexterity is needed for managing small to medium products.
• Exposure to oil, grease, occupational noise, cleaning solvents, dust, metal particles, sparks, coolant, and sharp-edged materials. Personal protective equipment (PPE) such as safety glasses, dust masks, ear plugs, cut-resistant or chemical-resistant gloves, and engineering controls may be required.
• Ability to sit or stand for prolonged periods