Job Summary
We are seeking a Clean Room Associate for a contract/temporary opportunity in Newbury Park, CA with a growing pharmaceutical team. This hands-on role is ideal for someone who is detail-oriented, dependable, and committed to following procedures in a regulated clean room environment.
This opportunity offers the chance to work in a collaborative, close-knit setting where quality, accountability, and teamwork are highly valued. As part of a smaller pharmaceutical environment, your contributions will be visible and meaningful. You will work alongside supportive teammates and leadership, gain exposure to GMP operations, and have opportunities to learn new responsibilities as the organization continues to grow.
Key Responsibilities
- Perform manufacturing and laboratory support activities within controlled clean room environments.
- Follow SOPs, GMP requirements, safety procedures, aseptic practices, and clean room protocols.
- Clean, sanitize, organize, and maintain clean room areas, equipment, materials, and supplies.
- Prepare and stage materials for manufacturing activities while supporting smooth daily operations.
- Complete batch records, logbooks, checklists, and other required documentation accurately and on time.
- Monitor conditions, report deviations or equipment issues, and communicate concerns to appropriate team members.
Compensation and Benefits
- Pay range: $22.00 to $25.00 per hour.
- Employment type: Contract/Temporary.
- 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.
Required Qualifications and Skills
- Support clean room manufacturing and laboratory operations in a regulated pharmaceutical environment.
- Maintain clean room cleanliness, sanitation, material staging, and documentation standards.
- Follow GMP, SOP, safety, gowning, and aseptic procedure requirements.
- Communicate operational concerns, deviations, and equipment issues to Manufacturing, Quality, and other team members.
- High school diploma or equivalent required.
- 1 to 2 years of relevant experience preferred in pharmaceutical, biotech, medical device, food manufacturing, laboratory, or another regulated environment.
- Strong attention to detail and commitment to accurately following written procedures.
- Comfortable working in a clean room environment and wearing required PPE and gowning.
- Ability to complete records, checklists, batch documentation, and logbooks accurately.
- Reliable, dependable, and willing to learn in a fast-paced environment.
- Strong communication skills, teamwork mindset, and positive attitude.
Preferred Qualifications
- Relevant college coursework, technical training, or education in science, manufacturing, biotechnology, pharmaceuticals, or a related field.
- Previous experience with GMP documentation, batch records, clean room protocols, or aseptic practices.
- Experience working with Manufacturing, Quality, or laboratory teams in a regulated production setting.