RIF. 3687 : REGULATORY AFFAIRS PROJECT MANAGER Our client is a Multinational Consumer Health Company. Role responsibilities : - End-to-end management of regulatory projects, ensuring timely submissions and successful approvals. - Participation in cross-functional projects, serving as the LOC Regulatory first point of contact for QSC, CMC, CMO, and internal manufacturing sites. - Management of local product information updates in accordance with GDS, acting as the LOC Regulatory first point of contact with the global labelling team. - Management of medicinal product upgrades, such as new indications, switching RX to OTC, formulation improvements, and new claims. Qualifications & Skills - Relevant previous experience (6 years) in a pharmaceutical or healthcare company. - Strong knowledge of pharmaceutical laws and regulations, with fluent management of the product lifecycle. - Knowledge of the fundamentals of medical devices. - Scientific degree (Pharmacy, Pharmaceutical Chemistry, Chemistry, or related disciplines). Preferred qualities - Good team player with strong interpersonal skills for effective cross-functional collaboration. - Spirit of continuous improvement and innovation, open to new ideas and methods. - Results-driven mindset and problem-solving skills. - Ability to work in a fast-paced, dynamic environment, managing multiple priorities. J-18808-Ljbffr