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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.
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