- Manage global product registrations and approvals, including compiling and submitting regulatory dossiers.
- Oversee the preparation 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 and approve product labels, packaging, and promotional materials to ensure compliance with regional regulations.
- Monitor and communicate changes in global regulatory requirements relevant to dietary supplements.
- Develop and deliver training sessions to internal teams on regulatory updates and best practices.
- Plan and execute global regulatory activities necessary to obtain and maintain regulatory approvals in international markets.
- 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.
- Develop and implement global regulatory strategies to ensure compliance for new and existing supplement products.
- 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 7-10 years of regulatory affairs experience.Fluent of English language written & spoken.Strong understanding of regulatory frameworks, product registration processes, and labeling requirements.Excellent communication, negotiation, and interpersonal skills.Proficiency in regulatory submission platforms and Microsoft Office Suite.