Production Line Lead - Medical Devices (2nd Shift)

VitalPath; Fort Snelling Unorganized Territory (MN); On-site; USD 30,000 - 40,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

HSA with company contribution

401K with company match

Paid time off

Parental leave

Job summary

VitalPath in Maplewood, MN is seeking a Production Line Lead to manage a small team on the second shift, guiding assembly of catheter components while ensuring quality and GMP standards.

You will train operators, monitor process adherence, and drive continuous improvement initiatives in a fast-paced manufacturing environment, with on-site responsibilities and close collaboration with Shift Supervisor to meet production goals.

Qualifications

• High school diploma or equivalent or related work experience.
• Understand blueprints/specifications preferred.
• 1–3 years medical device experience in clean room.
• ISO 13485 and cGMP knowledge preferred.
• Able to lift up to 50 lbs and sit for extended periods.

Responsibilities

• Lead a production team on an as-needed basis and oversee material requests and verification.
• Assist team in manufacturing parts and troubleshoot when needed.
• Ensure 100% adherence to manufacturing processes and documentation; support root cause investigations as needed.
• Maintain cGMP compliance, including labeling and documentation; conduct daily in-process inspections.
• Collect and report data to Shift Supervisor and contribute to 75% of production time.
• Identify continuous improvement initiatives and work with Shift Supervisor to implement changes.
• Perform additional duties as assigned.

Skills

Medical device manufacturing

Blueprint reading

Metric conversions

ISO 13485 knowledge

cGMP knowledge

Teamwork

Safety awareness

English proficiency

Education

High school diploma or equivalent

Tools

Excel

Word

Job description

VitalPath in Maplewood, MN is seeking a Production Line Lead to manage a small team on the second shift, guiding assembly of catheter components while ensuring quality and GMP standards.

You will train operators, monitor process adherence, and drive continuous improvement initiatives in a fast-paced manufacturing environment, with on-site responsibilities and close collaboration with Shift Supervisor to meet production goals.