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Assembler I 1st shift

Job in Irvine, Orange County, California, 92713, USA
Listing for: Marquee Staffing
Full Time position
Listed on 2026-08-06
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Production QC/QA
  • Quality Assurance - QA/QC
    Quality Engineering, Production QC/QA
Salary/Wage Range or Industry Benchmark: 19 - 20 USD Hourly USD 19.00 20.00 HOUR
Job Description & How to Apply Below

Contract to Hire $19 - $20/hr

Shifts:

1st shift Monday - Thursday 5:00am - 3:30pm

Summary/Objective

Medical Device implant manufacturer in Irvine is seeking applicants with manufacturing experience to join their team! Facilitating the manufacturing of insulin pump implants, this position will primarily perform precision assembly requiring, attention to detail, initiative, working well within a team, and ability to produce consistently high-quality results while using a microscope in a cleanroom environment.

Essential Duties and Responsibilities
  • Support company goals and objectives, policies and procedures, Good Manufacturing Practices, and FDA regulations including compliance to EN ISO 13485, Medical Device Quality Standards. Comply with company Standard Operating Procedures (SOPs) and departmental policies and procedures (DOPs), objectives, the quality assurance program, as well as safety and environmental standards.
  • Ability to establish, build and maintain professional working relationships with all levels of staff, clients, and suppliers.
  • Excellent interpersonal, verbal, and written communication skills.
  • Meticulous attention to detail and meeting deadlines.
  • Ability to learn new equipment and processes, and quickly demonstrate proficiency in their operation.
  • Read and interpret manufacturing procedures, engineering drawings, and inspection procedures and comply with their requirements. All documents are written in English.
  • Demonstrates accuracy, thoroughness and monitors own work to ensure quality.
  • Practice and always advocate good safety skills.
Education and Experience
  • Experience in FDA/GMP/ISO environment preferred
  • Excellent interpersonal, verbal, and written communication skills.
  • Meticulous attention to detail Wears personal protective equipment as required.
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