2nd Shift Medical Device Assembler - Precision & QA

Merrimack Manufacturing

California (MO)

On-site

USD 42,000 - 62,000

Full time

47 hours ago
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Job summary

Merrimack Manufacturing is seeking a reliable 2nd Shift Manufacturing Technician to assemble medical devices with meticulous attention to detail. The role covers assembly, testing and documentation of mechanical and electrical components in a clean-room environment.

The candidate will work Monday to Friday, 3:00 pm–12:15 am (9/80 schedule with every other Friday off), using various tools and equipment while ensuring compliance with GMP, ISO, QSR and FDA guidelines.

Qualifications

  • Minimum 2 years hands-on experience in a manufacturing environment.
  • Experience with assembly, testing and the documentation of mechanical and electrical devices.
  • Excellent interpersonal, verbal, and written communication skills.
  • Willingness to undertake varied tasks and adapt to dynamic environments.
  • Medical device manufacturing experience preferred.

Responsibilities

  • Assemble plastic and metal components into medical devices per procedures.
  • Utilize small hand tools, presses, fixtures, and measurement equipment to assemble and test.
  • Record results using BOMs, work orders, check sheets, and assembly drawings.
  • Conduct routine startup/end-of-day equipment inspections and verifications.
  • Maintain clean room integrity and safety practices; participate in continuous improvement.

Skills

Attention to detail
Self-sufficiency
Manual dexterity

Tools

Hand tools
Measurement equipment
Test fixtures
Soldering
Crimping
Ultrasonic welding

Job description

Merrimack Manufacturing is seeking a reliable 2nd Shift Manufacturing Technician to assemble medical devices with meticulous attention to detail. The role covers assembly, testing and documentation of mechanical and electrical components in a clean-room environment.

The candidate will work Monday to Friday, 3:00 pm–12:15 am (9/80 schedule with every other Friday off), using various tools and equipment while ensuring compliance with GMP, ISO, QSR and FDA guidelines.

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