Job Description
Our client is a leader in regenerative skincare with over 30 years of research, offering innovative, DNA-based solutions for both professional treatments and daily use. This is a unique opportunity to join a fast-growing company and contribute to its growth from the ground up.
Title: QA/RA Specialist
Location: Los Angeles, CA
Pay: $40/hr
Contract: 6-Month Contract-to-Hire
Job Summary:
Seeking an experienced QA/RA Specialist to support quality and regulatory operations in an FDA-regulated personal care/cosmetic manufacturing environment. This role involves overseeing compliance programs, managing audits, maintaining GMP documentation, handling product registrations, and supporting new product development.
Key Responsibilities:
- Maintain and implement GMP documentation (SOPs, batch records, validations, etc.)
- Oversee internal and external audits (FDA, state/local agencies)
- Conduct cGMP compliance audits and monitor manufacturing practices
- Manage regulatory filings, product registrations (OTC), and label reviews
- Handle customer complaints, CAPA investigations, and root cause analysis
- Ensure domestic and international regulatory compliance (FDA, EU, Canada, Asia)
- Support product development from design to launch with QA oversight
- Operate and review lab equipment/testing for raw materials and finished products
Qualifications:
- Bachelor’s in Life Science, Chemistry, or related field
- 5+ years QA/RA/QC experience in FDA-regulated cosmetic/personal care environment
- Strong knowledge of GMP, FDA, and global regulatory requirements
- Proficient in technical writing, documentation, and compliance reporting
- Skilled in auditing, complaint handling, and cross-functional collaboration
- Proficient with MS Office and Google Workspace
Job Tags
Contract work, Local area,