Job descriptionRegister global product and approvals, including compiling and submitting regulatory dossiers.prepare and review of technical documents (e.g., ingredient specifications, label claims, safety assessments).Liaise with regulatory authorities to facilitate product approvals and address queries.Review product labels, packaging, and promotional materials to ensure compliance with regional regulations.Monitor and communicate changes in global regulatory requirements relevant to dietary supplements.Assist in keeping company informed of regulatory requirements and external standards in international markets.Prepare International submissions and obtain product approval / clearance to include assistance with government queries and registration documentation requirements.Review Change Orders and assess regulatory impact of product changes on International regulatory strategy and submissions per standard procedures.Support post market regulatory compliance activities for international product approvals.Advise internal stakeholders (R&D, Marketing, Quality, Legal) on regulatory requirements affecting product development and marketing.Bachelor's Degree in Pharmaceutical Sciences, Nutrition, Science, or a related field.Experience in Dietary Supplements is a plus.Minimum of 3-6 years of regulatory affairs experience.Fluent of English language written & spoken.Strong understanding of regulatory frameworks, product registration processes, and labeling requirements.