R&D Regulatory Affairs Manager
24 Seven
- Englewood, NJ
- Permanent
- Full-time
- Participate in project teams in assigned categories to ensure completion of appropriate documents during the development process through final formula approval and launch
- Maintain and ensure compliance with the company ingredient policies and appropriate product regulations
- Ensure claims are compliant with the company and local regulatory requirements and consistent across labels, advertising, and other consumer communications
- Review and approve NA artworks
- Responsible for US regulatory submissions, including FDA drug and establishment registrations, supplement notifications, WERCS and EPA and state pesticide registrations
- Assist monitoring US state and federal regulations impacting the cosmetic and personal care industry including OTC
- Support with upcoming changes in the regulations including any specific monitoring and implementation for states, e.g., California
- Scientific degree preferred
- Over 5 years of Regulatory Affairs experience within a regulated industry, preferably skin and personal care products including OTC.
- Product development experience strongly preferred.
- Skin and personal care including OTC claim review experience strongly preferred.
- Track record adhering to compliance requirements (i.e. FDA, Health Canada, EPA, FTC, cGMP, ISO, etc.)
- Strong written communication skills, especially detail oriented and technical material.
- Experience communicating with cross-functional teams and customers including verbal presentations.
- Ability to work effectively both independently and as part of a team.
- Ability to meet deadlines while being flexible to changes in priorities and interruptions.
- Excellent organizational and analytical skills to complete assignments accurately.
- Full usability of MS Office suite (Excel, Word, Outlook, Powerpoint)