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Regulatory Affairs Specialist

Health Genesis Corp • Davie, FL, US • published 2026-09-24 22:03:54.974150

Description

We are seeking an experienced **Regulatory Affairs Specialist** to lead and support Product Development, Research \& Development (R\&D), Quality Assurance, Quality Control, and Regulatory Affairs within a nutraceutical manufacturing environment. This role is responsible for supporting new product development and commercialization, strengthening quality systems, overseeing regulatory compliance, and ensuring operations meet FDA, cGMP, applicable **21 CFR requirements**, and industry certification standards. The ideal candidate has strong experience in nutraceutical manufacturing, quality systems, regulatory compliance, product development, and cross\-functional project management. Key ResponsibilitiesProduct Development \& R\&D * Support new product development projects from development through commercialization. * Manage projects involving dietary supplements, gummies, liquids, capsules, powders, tablets, OTC products, and other dosage forms. * Ensure development activities meet quality, manufacturing, regulatory, and business requirements. * Coordinate with R\&D, QA/QC, Production, Operations, Marketing, and Sales to support successful product launches. * Support laboratory activi...

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