Process Operator I

We are hiring a Process Operator 1! Join our team in Berlin, CT!

Summary of Position:

Reporting to the Department Manager, this position will have direct responsibility for the processing of parts through various functions within the Department. TOMZ manufactures parts via high precision metal machining, finishing, assembly, and anodize processes for Medical Devices. The successful candidate will be expected to maintain the ISO 13485 standards documentation, prepare materials to be processed through various operations, and perform basic visual and dimensional inspections on completed components.

Essential Functions:

• Prepare and process components through various metal finishing operations.

Tumbling

Blasting

Heat Treat

Laser Welding

Laser Marking

Passivation

Anodize

• Perform visual and basic dimensional inspections on completed components, as required using micrometers, calipers, microscope, etc.
• Completes and compiles necessary documentation related to Quality Inspection standards.
• Ensure proper material control, identification and traceability is maintained for conforming and nonconforming material through the manufacturing processes.
• Support Quality Best Practices and GDP/GMP continuous improvement efforts.
• Utilize and navigate ERP and QMS systems to ensure inspection and traceability activities are properly documented and controlled, as needed.
• Must follow occupational Safety and Health requirements including Personal Protective Equipment (PPE) guidance and rules.
• Adhere to the TOMZ Quality Management System.
• Perform other duties as assigned.

Qualifications:

• Ability to use basic hand-held tools to support preventive maintenance activities.
• Maintains accuracy and attention to detail at all times and completes tasks in a timely manner.
• Strong background concerning the usage and care of mechanical metal finishing equipment and processes.
• Must have good organizational skills.

Education:

• High school diploma, GED, or equivalent directly transferrable work experience (Manufacturing or Engineering discipline preferred).

Experience:

• Minimum of 6 months-2 years’ experience in a regulated manufacturing environment.

Preferred Skills:

• Ability to effectively read and understand blueprints, specifications, and procedures.
• Knowledge of and experience with GMP/ISO standards.
• Regulated manufacturing industry experience (e.g. Aerospace, Defense, Pharmaceutical, etc.)
• Strong verbal and written English language communication skills.
• Class I, II and/or III Medical Device manufacturing experience

Physical Requirements:

• Ability to bend, stoop, squat, kneel, and lift up to 25 pounds. Team lift or mechanical assistance required for objects over 25 pounds.
• 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.