Regulatory Affairs Specialist

About this task

Responsibilities:
- Manage product registration and renewal in Egypt with the relevant regulatory authorities.
- Prepare, review, and submit regulatory dossiers and required documentation for new and existing products.
- Ensure product formulations, ingredients, claims, labels, packaging, and promotional materials comply with Egyptian regulatory requirements.
- Monitor changes in Egyptian regulations and regulatory guidelines relevant to supplements, nutraceuticals, vitamins, and consumer health products, and communicate their impact internally.
- Coordinate with R&D, Quality, Medical, Marketing, Supply Chain, and Commercial teams to ensure regulatory requirements are considered throughout the product lifecycle.
- Review artwork, labeling, claims, and marketing materials from a regulatory perspective and provide approvals or recommendations.
- Manage product variations, renewals, amendments, and post-registration activities.
- Maintain accurate and up-to-date regulatory files, certificates, approvals, licenses, and product documentation.
- Liaise with Egyptian regulatory authorities and relevant external parties regarding submissions, approvals, queries, and regulatory requirements.
- Support the regulatory assessment of new products, ingredients, formulations, and product claims before launch.
- Track regulatory submissions and approval timelines and follow up on pending actions.
- Identify potential regulatory risks and provide practical recommendations to support business continuity and product launches.

Requirements:
- Bachelor's degree in Pharmacy and Pharmaceutical Sciences.
- 1–2 years of experience in Regulatory Affairs, preferably within consumer health, nutraceuticals, or food supplements.

Employment type: Full-time.
Location: Giza, El Omraniya, Egypt.