Rif. 3687 : Regulatory Affairs Project Manager

RIF. 3687 : REGULATORY AFFAIRS PROJECT MANAGER Our client is a Multinational Consumer Health Company. Role responsibilities : E2E management of regulatory projects, ensuring timely submission and successful approval. Participate in cross-functional projects, serving as the LOC Regulatory first point of contact for QSC, CMC, CMO, and internal manufacturing sites. Manage local product information updates in accordance with GDS, acting as the LOC Regulatory first contact with the global labelling team. Oversee medicinal product upgrades, such as new indications, switching from 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 medical devices fundamentals. Scientific Degree (e.g., Pharmacy, Pharmaceutical Chemistry, Chemistry, or related disciplines). Preferred Good team player with strong interpersonal skills for effective cross-functional collaboration. Open to continuous improvement and innovation, embracing new ideas and methods. Results-driven with strong problem-solving skills. Ability to operate in a fast-paced, dynamic environment managing multiple priorities. J-18808-Ljbffr

Location: provincia-di-milano, IT

Posted Date: 6/13/2025