Assembler - 3/12 Work Schedule

Aerotek; Irvine (CA); On-site; USD 30,000 - 39,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) plan

Life insurance

Job summary

Aerotek is seeking an Assembler for a 3/12 schedule in Irvine, CA. The role focuses on electro‑mechanical and cleanroom device assembly in a regulated production environment, requiring attention to detail and teamwork.

Responsibilities include following SOPs, reading engineering docs, using micrometers/calipers, and operating equipment to ensure product quality. Onsite, contract‑to‑hire with comprehensive benefits may apply.

Qualifications

• Minimum of 2 years of medical device assembly experience.
• Diploma or equivalent level of education.
• Proficiency in electro‑mechanical assembly and cleanroom device assembly and packaging.
• Strong manual hand assembly skills with the ability to produce consistently high‑quality results.
• Ability to use basic hand tools, including micrometers, calipers, and other manual tools.
• Ability to operate electrical and mechanical equipment and interpret results accurately.
• Capability to read, interpret, and learn engineering drawings, manufacturing procedures, processes, and inspection procedures in English.
• Ability to work well with others in a cross‑functional team environment.
• Meticulous attention to detail and the ability to detect issues with tooling, materials, processes, and quality.
• Ability to work with minimal supervision while meeting deadlines and production targets.
• Ability to use a computer with various programs to transact product in the production system and complete online training.
• Clear verbal and written communication skills and strong active listening abilities.
• Commitment to following Good Manufacturing Practices, SOPs, DOPs, and medical device quality standards.
• Strong focus on safety and adherence to environmental and workplace safety standards.

Responsibilities

• Perform electro‑mechanical assembly and clean room device assembly and packaging in accordance with manufacturing procedures and quality standards.
• Support organizational goals, objectives, policies, and procedures, including Good Manufacturing Practices and applicable medical device quality standards.
• Comply with Standard Operating Procedures (SOPs), departmental policies and procedures (DOPs), quality assurance programs, and all safety and environmental standards.
• Read and interpret manufacturing procedures, engineering drawings, and inspection procedures written in English, and follow their requirements accurately.
• Use basic hand tools such as micrometers, calipers, and other manual tools to assemble and inspect components and finished products.
• Operate electrical and mechanical equipment as required and interpret results to ensure proper function and product quality.
• Monitor own work to ensure accuracy and thoroughness, consistently producing high‑quality results and identifying issues with tooling, materials, processes, or quality.
• Learn new equipment and processes quickly and demonstrate proficiency in their operation.
• Work with minimal supervision while maintaining productivity and adherence to production schedules and deadlines.
• Collaborate effectively with others in a cross‑functional team environment, establishing 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.
• Transact product within the production system using computer‑based programs and complete required online training.
• Practice and advocate good safety skills at all times, maintaining a clean and compliant work area within the cleanroom and production environment.

Skills

Medical device assembly

Teamwork

Attention to detail

Manual dexterity

Read engineering drawings

English procedures

Education

Diploma or equivalent

Tools

Micrometers

Calipers

Hand tools

Job description

Job Title: Assembler – 3/12 Work Schedule Shift

Job Description

The Assembler performs electro‑mechanical and clean room device assembly and packaging within a regulated medical device production environment. This role requires strong manual assembly skills, consistent attention to detail, and the ability to work effectively in a team while producing high-quality products. You will follow established procedures, operate basic hand tools and equipment, and support continuous growth as new products are introduced.

Responsibilities

• Perform electro‑mechanical assembly and clean room device assembly and packaging in accordance with manufacturing procedures and quality standards.

• Support organizational goals, objectives, policies, and procedures, including Good Manufacturing Practices and applicable medical device quality standards.

• Comply with Standard Operating Procedures (SOPs), departmental policies and procedures (DOPs), quality assurance programs, and all safety and environmental standards.

• Read and interpret manufacturing procedures, engineering drawings, and inspection procedures written in English, and follow their requirements accurately.

• Use basic hand tools such as micrometers, calipers, and other manual tools to assemble and inspect components and finished products.

• Operate electrical and mechanical equipment as required and interpret results to ensure proper function and product quality.

• Monitor own work to ensure accuracy and thoroughness, consistently producing high‑quality results and identifying issues with tooling, materials, processes, or quality.

• Learn new equipment and processes quickly and demonstrate proficiency in their operation.

• Work with minimal supervision while maintaining productivity and adherence to production schedules and deadlines.

• Collaborate effectively with others in a cross‑functional team environment, establishing 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.

• Transact product within the production system using computer‑based programs and complete required online training.

• Practice and advocate good safety skills at all times, maintaining a clean and compliant work area within the cleanroom and production environment.

Essential Skills

• Minimum of 2 years of medical device assembly experience.

• Diploma or equivalent level of education.

• Proficiency in electro‑mechanical assembly and cleanroom device assembly and packaging.

• Strong manual hand assembly skills with the ability to produce consistently high‑quality results.

• Ability to use basic hand tools, including micrometers, calipers, and other manual tools.

• Ability to operate electrical and mechanical equipment and interpret results accurately.

• Capability to read, interpret, and learn engineering drawings, manufacturing procedures, processes, and inspection procedures in English.

• Ability to work well with others in a cross‑functional team environment.

• Meticulous attention to detail and the ability to detect issues with tooling, materials, processes, and quality.

• Ability to work with minimal supervision while meeting deadlines and production targets.

• Ability to use a computer with various programs to transact product in the production system and complete online training.

• Clear verbal and written communication skills and strong active listening abilities.

• Commitment to following Good Manufacturing Practices, SOPs, DOPs, and medical device quality standards.

• Strong focus on safety and adherence to environmental and workplace safety standards.

Additional Skills & Qualifications

• Experience working in a cleanroom or controlled production environment.

• Familiarity with medical device manufacturing and packaging processes.

• Ability to quickly learn new equipment and processes and demonstrate proficiency.

• Strong interpersonal skills and the ability to build and maintain professional working relationships at all levels.

• Demonstrated ability to monitor and verify the quality of own work.

• Comfort working on a fixed weekend‑based schedule and extended shifts.

Why Work Here?

You will join a growing organization that is introducing new products and expects significant future growth, creating opportunities for professional development and advancement. The environment values quality, teamwork, and continuous learning, offering the chance to build skills in a regulated medical device setting while contributing to products that make a meaningful impact.

Work Environment

This role is based in a cleanroom and production environment focused on medical device manufacturing. You will work with electro‑mechanical equipment, basic hand tools such as micrometers and calipers, and computer‑based production systems. The position follows a 3/12 schedule, working Friday through Sunday from 5:00 a.m. to 5:30 p.m. The environment emphasizes adherence to safety, quality, and regulatory standards, with appropriate cleanroom practices and attire required.

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 $22.00 - $28.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job‑related factors.

Eligibility requirements apply to some benefits and may depend on your jobclassification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefitsavailable 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

Workplace Type

This is a fully onsite position in Irvine, CA.

Application Deadline

This position is anticipated to close on Oct 6, 2026.

About Aerotek

Aerotek Inc. provides staffing and services solutions in manufacturing, logistics, construction, aviation, facilities and maintenance. We provide the expertise, solutions and people required to rise to the challenges of North American industry. Headquartered in Hanover, Md., Aerotek operates a unified network of over 200 offices across North America, supporting more than 18,000 clients each year. Aerotek is an Allegis Group company, the global leader in workforce and business solutions.

Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.