Assembler

Assembler I

The Assembler I performs electro-mechanical assembly and clean room device assembly and packaging in a regulated medical device production environment. This role requires strong manual assembly skills, meticulous attention to detail, and the ability to consistently produce high-quality work while collaborating effectively within a cross-functional team.

Responsibilities

• Perform electro-mechanical assembly and clean room device assembly and packaging in accordance with documented procedures.
• Support organizational goals, objectives, policies, and procedures, including adherence to Good Manufacturing Practices and applicable medical device quality standards.
• Comply with Standard Operating Procedures (SOPs), departmental procedures (DOPs), quality assurance requirements, and all safety and environmental standards.
• Read and interpret manufacturing procedures, engineering drawings, and inspection procedures written in English, and follow them accurately during production.
• Use basic hand tools such as micrometers, calipers, and other measuring devices to assemble and verify components.
• Operate electrical and mechanical equipment as required and accurately interpret test and inspection results.
• Monitor personal work output to ensure accuracy, thoroughness, and consistent product quality, promptly identifying and reporting issues related to tooling, materials, processes, or quality.
• Learn new equipment, processes, and procedures and quickly demonstrate proficiency in their operation.
• Work with minimal supervision while maintaining productivity, quality, and compliance with all relevant standards.
• Collaborate effectively with colleagues in a cross-functional team environment, building and maintaining professional working relationships with staff, clients, and suppliers.
• Communicate clearly, both verbally and in writing, and demonstrate active listening to ensure effective coordination and problem solving.
• Use computer systems and various software programs to transact product within the production system and complete required online training.
• Practice and advocate safe work habits at all times, maintaining a clean, organized, and compliant work area.
• Participate in cross-training across multiple departments, including packaging, production, and cleanroom operations, and perform repetitive tasks with consistent focus and accuracy.

Essential Skills

• At least 1 year of medical device assembly experience.
• Diploma or equivalent education.
• Proven manual hand assembly skills in a production environment.
• Experience working in a cleanroom or controlled production environment.
• Ability to use basic hand tools such as micrometers, calipers, and other measuring instruments.
• Ability to operate electrical and mechanical equipment and accurately interpret results.
• Strong attention to detail with the ability to detect issues related to tooling, materials, processes, and quality.
• Ability to read, interpret, and learn engineering drawings, manufacturing procedures, and inspection procedures written in English.
• Ability to work well with others in a cross-functional team environment.
• Capability to work with minimal supervision while maintaining high quality and productivity.
• Proficiency using a computer and various programs to transact product within the production system and complete online training.
• Excellent interpersonal, verbal, and written communication skills.
• Ability to demonstrate active listening and respond clearly and professionally.
• Commitment to following safety, environmental, and quality standards at all times.

Additional Skills & Qualifications

• Previous experience in electro-mechanical assembly is an asset.
• Familiarity with medical device quality standards and Good Manufacturing Practices.
• Experience working under microscopes for detailed assembly or inspection.
• Comfort working in a highly regulated environment with documented procedures.
• Ability to adapt quickly to new equipment, processes, and departmental cross-training.
• Strong time management skills with the ability to meet deadlines in a production setting.

Why Work Here?

You will join a growing operation that is introducing a new product and anticipating significant expansion, creating opportunities for professional growth and cross-training across multiple departments. The environment promotes learning, collaboration, and skill development, allowing you to build a strong foundation in medical device manufacturing. You will work in a setting that values quality, safety, and continuous improvement, providing a stable platform for long-term career development.

Work Environment

This position is on a 4th shift schedule, working Friday through Sunday from 5:00 p.m. to 5:30 a.m., with three 12-hour shifts each week. The first workday typically starts on a Friday afternoon. The role is based in a cleanroom and production environment, with a mix of sitting and standing throughout the shift. You will be cross-trained in multiple departments, including packaging, production, and cleanroom operations, with approximately two weeks of training in each area. The work is highly repetitive and process-driven, requiring consistent focus, adherence to documented procedures, and comfort working with cleanroom protocols and production equipment.

Job Type & Location

This is a Contract to Hire position based out of Irvine, CA.

Pay and Benefits

The pay range for this position is $20.33 - $20.33/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Irvine, CA.

Application Deadline

This position is anticipated to close on Jun 3, 2026.