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CNC Swiss and Mill-Turn Operator — Regulated Manufacturing

Job in Berlin, Hartford County, Connecticut, 06037, USA
Listing for: Torrey Holistics
Full Time position
Listed on 2026-06-29
Job specializations:
  • Manufacturing / Production
    Production QC/QA, Quality Engineering
Salary/Wage Range or Industry Benchmark: 40000 - 60000 USD Yearly USD 40000.00 60000.00 YEAR
Job Description & How to Apply Below
CNC Swiss and Mill-Turn Operator — Regulated Manufacturing Help TOMZ build precision components for medical devices while upholding ISO 13485 and GMP expectations. In this role, you will be part of a quality-driven team, reporting to the Operations Supervisor and contributing to safe, reliable production.

Role highlights

Produce components on 3-, 4-, and 5-axis mills, mill-turns, and CNC Swiss platforms (Citizen, Tsugami), plus Index multi-spindle lathes and Robo Drills.

Inspect parts visually and dimensionally with microscope, micrometer, caliper, pin/thread gauges, comparator, and Micro-Hite.

Document results in ERP and QMS to maintain traceability and compliance with ISO 13485.Drive quality by following the TOMZ Quality Management System and supporting GDP/GMP continuous improvement.

Engage in problem-solving when complex machine or process issues arise.

Maintain safe work practices and PPE usage at all times.

Ensure proper material identification, control, and segregation of conforming vs. nonconforming product.

Perform other duties as assigned.

What you will work with Equipment:
Robo Drills, horizontal/vertical mills, mill-turns, CNC Swiss lathes (Citizen, Tsugami), Index multi-spindle lathes.

Metrology: microscope, micrometer, caliper, pin gauges, thread gauges, comparator, Micro-Hite.

Systems: ERP and QMS for inspection records and traceability control.

Your background

Basic knowledge of machine operation, care, and inspection processes.

Comfort using hand tools for preventive maintenance, repairs, and tool changes.

Ability to interpret blueprints, specifications, and procedures.

Detail-focused, accurate, and timely execution of tasks.

Introductory GD&T skills and familiarity with GMP/ISO standards.

Experience0-2 years in a regulated manufacturing environment.

Preferred Experience with Class I, II, and/or III medical device manufacturing.

Exposure to aerospace, defense, or pharmaceutical manufacturing environments.

Clear written and verbal communication in English.

Physical requirements

Able to bend, stoop, squat, kneel, and lift up to 50 pounds; team lift or mechanical assist required over 50 pounds.

Repetitive hand/arm motions while handling up to 20 pounds, including gripping, twisting, placing parts for extended periods, and overhead lifting.
20/20 vision (assisted or unassisted) needed to sort raw and non-conforming materials; good dexterity for small to medium products.

Comfort working around oil, grease, noise, cleaning solvents, dust, metal particles, sparks, and coolant; PPE and engineering controls may be required.

Ability to sit or stand for long durations.

Culture and safety

Our team is built on disciplined process control and continuous improvement. You will contribute to Quality Best Practices while following occupational safety guidelines and PPE rules to protect yourself and your teammates.
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