Support the execution of content and compliance processes.
Collaborate across teams to flag risks, provide regulatory guidance, and keep compliance activities moving.
Contribute to global regulatory and compliance strategy by owning key workstreams across labeling, claims substantiation, ingredient documentation, and product review.
Partner cross-functionally to support product development and brand initiatives.
Conduct ingredient, formula, and packaging compliance reviews according to regulatory frameworks, particularly the U.S. FDCA.
Maintain raw material and formula-level compliance documentation.
Execute compliance reviews consistent with FTC and FDA claims compliance standards.
Serve as day-to-day regulatory contact for Brand, Creative, and Marketing.
Contribute to, review and approve QMS records, particularly labels, formulas, specifications, and change controls.
Integrate Regulatory Affairs into generative AI workflows and maintain accurate customer service messaging.
Requirements
Minimum of 6 years experience in Regulatory Affairs in a GMP (Good Manufacturing Practices) environment, with at least 4 executing technical regulatory reviews in dietary supplements for the U.S.
Minimum B.Sc. in pharmaceutical, nutritional, or life sciences or a related scientific field.
Experience in attaining and adhering to compliance with FDA regulations, including 21 CFR 111 and FSMA.
Strong knowledge of the FDA regulatory landscape and enforcement discretion trends for dietary supplements.
Experience with structure/function claim compliance and general FTC advertising rules.
Strong knowledge of GMP product documentation requirements.
Strong knowledge of dietary supplement labeling requirements.
Experience representing regulatory positions in cross-functional teams.