Assembler II 1st shift

Marquee Staffing; Irvine (CA); On-site; USD 29,000 - 32,000; Full time

Job summary

Marquee Staffing seeks an experienced manufacturing professional for a contract-to-hire role in Irvine. The position focuses on precision assembly for insulin pump implants, requiring attention to detail, teamwork, and the ability to produce high-quality results while working under a microscope in a cleanroom environment.

The ideal candidate has at least 3+ years in medical device production, familiarity with FDA/GMP/ISO environments, and strong communication skills.

Qualifications

• 3+ years related industry experience in medical device production assembly.
• 3+ years of experience in a medical device environment
• Experience in FDA/GMP/ISO environment preferred
• Excellent interpersonal, verbal, and written communication skills.
• Meticulous attention to detail

Responsibilities

• Support company goals, SOPs, and FDA regulations including EN ISO 13485.
• Comply with SOPs and departmental policies, quality assurance program, safety and environmental standards.
• Ability to establish and maintain professional relationships with all levels of staff, clients, and suppliers.
• Demonstrate excellent interpersonal, verbal, and written communication skills.
• 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 advocate good safety skills.

Skills

Attention to detail

Communication skills

Teamwork

Learn new equipment

Job description

Contract to Hire $21.50/hr-$23.50 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

• 3+ years related industry experience in medical device production assembly.
• 3+ years of experience in a medical device environment
• Experience in FDA/GMP/ISO environment preferred
• Excellent interpersonal, verbal, and written communication skills.
• Meticulous attention to detail
• Wears personal protective equipment as required.