Precision Process Operator I - Medical Device Manufacturing

TOMZ Corporation; Berlin (CT); On-site; USD 42,000 - 52,000; Full time

Job summary

TOMZ Corporation in Berlin, CT is seeking a Process Operator 1 to support the manufacturing of medical device components. You will oversee processing of parts through metal finishing, inspection, and assembly, while ensuring accurate documentation and adherence to ISO 13485 standards.

The role requires basic hand-tools use, strong attention to detail, and good organizational skills. Familiarity with GMP/ISO requirements is preferred; training and growth opportunities are provided in a regulated,

Qualifications

• High school diploma or equivalent required or transferable manufacturing experience.
• Experience in a regulated manufacturing environment (6 months–2 years) preferred.
• Familiarity with GMP/ISO standards is a plus.

Responsibilities

• Perform visual and basic dimensional inspections on components using micrometers, calipers, microscope, etc.
• Complete and compile documentation related to Quality Inspection standards.
• Ensure material control, identification and traceability for conforming and nonconforming material through manufacturing processes.
• Support Quality Best Practices and GDP/GMP continuous improvement efforts.
• Utilize ERP and QMS systems to document inspection activities and controls.
• Follow PPE guidance and safety requirements and TOMZ Quality Management System.

Skills

Hand tools

Attention to detail

Organizational skills

Finishing equipment care

Education

High school diploma or GED

Tools

ERP systems

QMS software

Micrometers

Calipers

Job description

TOMZ Corporation in Berlin, CT is seeking a Process Operator 1 to support the manufacturing of medical device components. You will oversee processing of parts through metal finishing, inspection, and assembly, while ensuring accurate documentation and adherence to ISO 13485 standards.

The role requires basic hand-tools use, strong attention to detail, and good organizational skills. Familiarity with GMP/ISO requirements is preferred; training and growth opportunities are provided in a regulated,