Social network you want to login/join with: RIF. 3687: REGULATORY AFFAIRS PROJECT MANAGER, Pavia Client: Arethusa Location: Pavia Job Category: Other EU work permit required: Yes Job Reference: 67651728538861568033713 Job Views: 2 Posted: 06.06.2025 Expiry Date: 21.07.2025 Job Description: 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 submission and successful approval. Participating in cross-functional projects, serving as the LOC Regulatory first point of contact for QSC, CMC, CMO, and internal manufacturing sites. Managing local product information updates in accordance with GDS, acting as the LOC Regulatory first point of contact with the global labeling team. Managing medicinal product upgrades, such as new indications, switching RX to OTC, improved formulations, 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 lifecycle. Knowledge of medical devices fundamentals. Scientific degree (Pharmacy, Pharmaceutical Chemistry, Chemistry, or related disciplines). Preferred: Good team player with strong interpersonal skills for cross-functional collaboration. Spirit of continuous improvement and innovation, open to new ideas and methods. Results-driven with problem-solving skills. Ability to work in a fast-paced, dynamic environment, managing multiple priorities. J-18808-Ljbffr