Cleanroom Assembler

Job Summary

We are seeking Cleanroom Assemblers for urgent 1st and 2nd shift openings in Camarillo, CA.

The Cleanroom Assembler will support high-demand production by assembling components in a controlled environment while following strict quality, safety, and documentation standards. Qualified candidates with strong related cleanroom assembly experience may be considered for direct hire.

Key Responsibilities

- Assemble products and components in a cleanroom environment according to work instructions and quality standards.
- Follow ISO, GMP, cleanroom, and safety procedures to maintain compliance and product integrity.
- Inspect parts, materials, and finished assemblies for quality, accuracy, and defects.
- Wear required cleanroom garments, including a bunny suit, and follow contamination control practices.
- Complete production documentation accurately and communicate issues to leads or supervisors.
- Support production goals by working efficiently in a fast-paced manufacturing environment.

Compensation and Benefits

- Pay: $21 per hour for 1st shift.
- Pay: $22 per hour for 2nd shift.
- 1st shift openings: 5:00 AM to 1:30 PM or 6:00 AM to 2:30 PM.
- 2nd shift openings: 3:00 PM to 11:30 PM.
- Some overtime may be required.
- Location: Camarillo, CA.
- Job type: Direct hire opportunity for qualified candidates.
- Benefits once hired may include medical, dental, vision, HSA, FSA, life insurance, AD&D, short-term disability, long-term disability, EAP, life referrals, and 401(k)/Roth with company match.

Equal Opportunity Employer / Disabled / Protected Veterans

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For temporary assignments lasting 13 weeks or longer, AppleOne is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.

We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team.

AppleOne participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program.

We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

Additional Skills

Required Qualifications and Skills

- Perform cleanroom assembly of products and components in a regulated manufacturing environment.
- Follow written work instructions, production procedures, and quality standards.
- Inspect completed assemblies and maintain accurate production documentation.
- Support daily production targets while maintaining safety, cleanliness, and compliance.

- 1 to 2 years of assembly, manufacturing, production, or cleanroom experience preferred.
- Experience working in a cleanroom, ISO, GMP, medical device, biotech, pharmaceutical, or other regulated environment is highly desired.
- Must be comfortable wearing full cleanroom attire, including a bunny suit.
- Ability to perform detailed assembly work with accuracy and consistency.
- Strong attendance, reliability, and work history are important.
- Ability to work in a fast-paced production environment and follow instructions closely.
- Must be able to pass a background check.

Preferred Qualifications

- Prior cleanroom assembly experience in a regulated manufacturing environment.
- Experience with medical device, life sciences, biotech, pharmaceutical, or high-quality precision assembly.
- Stable work history with demonstrated longevity in previous roles.
- Familiarity with ISO, GMP, quality documentation, and contamination control procedures.