Assembler
Aerotek, Irvine, CA, United States
Assembler I
The Assembler I performs electro-mechanical and clean room device assembly and packaging for medical devices in a regulated production environment. This role relies on strong manual assembly skills, meticulous attention to detail, and the ability to consistently deliver high-quality work while collaborating effectively within a cross-functional team.
This is a 4/10 schedule, Monday through Thursday, 5am to 3:30pm. They will be cross trained and candidates must be open to working on different lines/departments.
Responsibilities include performing electro-mechanical assembly and clean room device assembly according to established manufacturing procedures and engineering drawings. Packaging medical devices in compliance with applicable procedures, quality standards, and regulatory requirements. Supporting company goals, objectives, policies, procedures, Good Manufacturing Practices, and FDA regulations, including compliance with medical device quality standards. Following and adhering to company Standard Operating Procedures (SOPs), departmental operating procedures (DOPs), quality assurance programs, and safety and environmental standards. Reading, interpreting, and following manufacturing procedures, engineering drawings, and inspection procedures written in English, ensuring all requirements are met. Using basic hand tools, micrometers, calipers, and other equipment to assemble and verify components and products. Operating electrical and mechanical equipment and accurately interpreting results to support production and quality requirements. Monitoring work output for accuracy and completeness, demonstrating thoroughness and a strong focus on quality. Identifying and reporting issues with tooling, materials, processes, or product quality and contributing to resolving them. Learning new equipment and processes quickly and demonstrating proficiency in their operation within the production environment. Transacting product within the production system and completing required online training using computer-based programs. Communicating clearly and professionally with team members and other departments, both verbally and in writing, and demonstrating active listening. Establishing, building, and maintaining professional working relationships with staff, clients, and suppliers. Working effectively with minimal supervision while contributing positively to a cross-functional team. Practicing and advocating good safety skills at all times, maintaining a clean and organized work area.
Essential skills include at least 2 years of medical device assembly experience. Proficiency in electro-mechanical assembly and clean room production processes. Strong manual hand assembly skills with a high level of dexterity. Ability to read and interpret engineering drawings, manufacturing procedures, and inspection procedures in English. Experience working in a cleanroom and production environment. Ability to use basic hand tools, including micrometers, calipers, and similar measuring devices. Ability to operate electrical and mechanical equipment and accurately interpret results. Strong attention to detail with a focus on producing consistently high-quality work. Ability to detect and respond to issues with tooling, materials, processes, and quality. Ability to work well with others in a cross-functional team environment. Capability to work with minimal supervision while meeting deadlines. Effective interpersonal, verbal, and written communication skills. Ability to use a computer and various software programs to transact product and complete online training.
Additional skills and qualifications include a diploma or equivalent level of education. Familiarity with Good Manufacturing Practices and FDA regulations for medical devices. Experience adhering to Standard Operating Procedures (SOPs), departmental operating procedures (DOPs), and quality assurance programs. Demonstrated initiative and willingness to learn new equipment, processes, and systems. Ability to build and maintain professional working relationships with staff, clients, and suppliers. Strong sense of ownership for work quality and personal performance. Commitment to safety and environmental standards in a production setting.
Why work here? You will join a growing organization that is introducing new products and creating strong opportunities for professional development and advancement. The environment encourages learning new equipment and processes, expanding your technical skills, and working closely with a supportive, cross-functional team. You will contribute directly to high-quality medical devices that make a meaningful impact, while benefiting from a culture that values initiative, collaboration, and continuous improvement.
Work environment is based in a cleanroom and production environment dedicated to medical device manufacturing. You will work with electro-mechanical equipment, basic hand tools, micrometers, calipers, and computer-based systems to support production and quality activities. The position requires adherence to strict cleanliness, safety, and environmental standards, as well as compliance with documented procedures and regulatory requirements. Work is team-oriented yet allows for independent task execution under minimal supervision, with an emphasis on accuracy, consistency, and product quality.
Job type and location is a contract to hire position based out of Irvine, CA. Pay and benefits range from $19.00 to $19.00/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 is a fully onsite position in Irvine, CA. Application deadline is anticipated to close on May 12, 2026.
The Assembler I performs electro-mechanical and clean room device assembly and packaging for medical devices in a regulated production environment. This role relies on strong manual assembly skills, meticulous attention to detail, and the ability to consistently deliver high-quality work while collaborating effectively within a cross-functional team.
This is a 4/10 schedule, Monday through Thursday, 5am to 3:30pm. They will be cross trained and candidates must be open to working on different lines/departments.
Responsibilities include performing electro-mechanical assembly and clean room device assembly according to established manufacturing procedures and engineering drawings. Packaging medical devices in compliance with applicable procedures, quality standards, and regulatory requirements. Supporting company goals, objectives, policies, procedures, Good Manufacturing Practices, and FDA regulations, including compliance with medical device quality standards. Following and adhering to company Standard Operating Procedures (SOPs), departmental operating procedures (DOPs), quality assurance programs, and safety and environmental standards. Reading, interpreting, and following manufacturing procedures, engineering drawings, and inspection procedures written in English, ensuring all requirements are met. Using basic hand tools, micrometers, calipers, and other equipment to assemble and verify components and products. Operating electrical and mechanical equipment and accurately interpreting results to support production and quality requirements. Monitoring work output for accuracy and completeness, demonstrating thoroughness and a strong focus on quality. Identifying and reporting issues with tooling, materials, processes, or product quality and contributing to resolving them. Learning new equipment and processes quickly and demonstrating proficiency in their operation within the production environment. Transacting product within the production system and completing required online training using computer-based programs. Communicating clearly and professionally with team members and other departments, both verbally and in writing, and demonstrating active listening. Establishing, building, and maintaining professional working relationships with staff, clients, and suppliers. Working effectively with minimal supervision while contributing positively to a cross-functional team. Practicing and advocating good safety skills at all times, maintaining a clean and organized work area.
Essential skills include at least 2 years of medical device assembly experience. Proficiency in electro-mechanical assembly and clean room production processes. Strong manual hand assembly skills with a high level of dexterity. Ability to read and interpret engineering drawings, manufacturing procedures, and inspection procedures in English. Experience working in a cleanroom and production environment. Ability to use basic hand tools, including micrometers, calipers, and similar measuring devices. Ability to operate electrical and mechanical equipment and accurately interpret results. Strong attention to detail with a focus on producing consistently high-quality work. Ability to detect and respond to issues with tooling, materials, processes, and quality. Ability to work well with others in a cross-functional team environment. Capability to work with minimal supervision while meeting deadlines. Effective interpersonal, verbal, and written communication skills. Ability to use a computer and various software programs to transact product and complete online training.
Additional skills and qualifications include a diploma or equivalent level of education. Familiarity with Good Manufacturing Practices and FDA regulations for medical devices. Experience adhering to Standard Operating Procedures (SOPs), departmental operating procedures (DOPs), and quality assurance programs. Demonstrated initiative and willingness to learn new equipment, processes, and systems. Ability to build and maintain professional working relationships with staff, clients, and suppliers. Strong sense of ownership for work quality and personal performance. Commitment to safety and environmental standards in a production setting.
Why work here? You will join a growing organization that is introducing new products and creating strong opportunities for professional development and advancement. The environment encourages learning new equipment and processes, expanding your technical skills, and working closely with a supportive, cross-functional team. You will contribute directly to high-quality medical devices that make a meaningful impact, while benefiting from a culture that values initiative, collaboration, and continuous improvement.
Work environment is based in a cleanroom and production environment dedicated to medical device manufacturing. You will work with electro-mechanical equipment, basic hand tools, micrometers, calipers, and computer-based systems to support production and quality activities. The position requires adherence to strict cleanliness, safety, and environmental standards, as well as compliance with documented procedures and regulatory requirements. Work is team-oriented yet allows for independent task execution under minimal supervision, with an emphasis on accuracy, consistency, and product quality.
Job type and location is a contract to hire position based out of Irvine, CA. Pay and benefits range from $19.00 to $19.00/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 is a fully onsite position in Irvine, CA. Application deadline is anticipated to close on May 12, 2026.