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Regulatory Affairs Specialist
California, Kentucky, United States · Full Time
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- Experience
- 1+ yrs
- Salary
- —
- Openings
- 1
- Posted
- 1 week ago
- Work mode
- In office
- Education
- Bachelor's degree
- Resume
- Required to apply
Where you'll work
Job description
Overview
We are collaborating with a prominent personal care and cosmetics manufacturer located in the Los Angeles Metropolitan area to find a skilled Regulatory Affairs Specialist.
Key Duties
- Create and maintain detailed product dossiers for all manufactured items.
- Gather, evaluate, and organize documentation related to packaging, components, raw materials, batch records, and safety data sheets.
- Ensure compliance with U.S. MoCRA regulations, cosmetic labeling standards, and international regulatory requirements.
- Communicate regulatory guidelines and standards concerning cosmetics to internal teams.
- Maintain tracking systems for regulatory inquiries, submissions, and information requests.
- Collaborate with research and development, quality control, production, and other departments to guarantee accurate and comprehensive regulatory documentation.
Candidate Qualifications
- Bachelor’s degree in a relevant field or equivalent qualification.
- Minimum of one year experience in a related regulatory role.
- Strong skills in Microsoft Excel, Word, and Outlook.
- Capability to prioritize and handle multiple tasks efficiently within a dynamic manufacturing environment.
Offer and Benefits
- Competitive base salary package.
- Attractive benefits including medical insurance, 401(k) matching, paid time off, and shortened Fridays.
- Flexible working hours and a well-regarded company culture.
Skills
Cross-functional Collaboration
Regulatory Compliance
Microsoft Word Proficiency
Microsoft Excel proficiency
Microsoft Outlook proficiency
Product dossier management
Cosmetic labeling regulations
Documentation review and organization
Knowledge of U.S. MoCRA regulations
Time management in manufacturing