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Cleanroom Production Associate

Job ID: 1804978
Reference Code: DF-Cleanroom-Production Associate

  • $47,800 to $52,000
  • Newbury Park, 91320

Job Summary

A leading pharmaceutical manufacturing environment in Newbury Park, CA is seeking dependable and detail-oriented Cleanroom Production Associates for a temp-to-hire opportunity. This role is ideal for candidates with cleanroom, GMP, biotech, pharmaceutical, medical device, or regulated production experience who are looking to grow in a stable, quality-focused industry.

As a Cleanroom Production Associate, you will support daily production and assembly activities in a highly regulated cleanroom setting. This opportunity offers a team-oriented work environment, supportive leadership, and the chance to build long-term skills in pharmaceutical manufacturing. Candidates who take pride in accuracy, consistency, safety, and documentation will be well-positioned for success.

Key Responsibilities

- Perform production, assembly, and packaging activities in a regulated cleanroom environment.
- Follow SOPs, GMP requirements, gowning procedures, and quality control standards.
- Complete accurate production documentation in compliance with established procedures.
- Inspect products, components, and materials for quality, consistency, and compliance.
- Maintain clean, organized work areas and follow all safety and contamination control requirements.
- Work collaboratively with team members to meet daily production goals and quality expectations.

Compensation and Benefits

- Pay range: $23.00 to $25.00 per hour.
- Employment type: Temp-to-hire.
- Location: Newbury Park, CA.



Equal Opportunity Employer / Disabled / Protected Veterans

The Know Your Rights poster is available here:
https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf

The pay transparency policy is available here:
https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf

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.
https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf

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 production and assembly tasks in a regulated pharmaceutical manufacturing environment.
- Follow GMP, SOP, safety, gowning, and documentation procedures.
- Inspect products and materials to support quality and compliance standards.
- Maintain productivity while performing repetitive, detail-focused production work.

- 1 to 2 years of relevant production, cleanroom, pharmaceutical, biotech, medical device, or regulated manufacturing experience preferred.
- Familiarity with GMP requirements, SOPs, and cleanroom procedures.
- Strong attention to detail and ability to complete accurate documentation.
- Reliable attendance and ability to follow structured production processes.
- Comfortable performing repetitive tasks while maintaining quality and consistency.
- Ability to work effectively in a regulated, quality-focused team environment.

Preferred Qualifications

- Previous cleanroom experience in pharmaceutical, biotech, medical device, or other regulated manufacturing environments.
- Prior experience following gowning procedures and contamination control practices.
- Experience completing batch records, production logs, or similar manufacturing documentation.

AppleOne Representative Contact Info

Account Executive:
Dawn
Branch Phone:
Location:
Thousand Oaks, CA