offres d’emploi chez MD à Italie

This position is with Meditrial Europe Ltd., located in Rome, Italy. The role requires EU work permit approval and is office-based with potential travel.

• Job Reference: d44949a5bc97
• Job Views: 2
• Posted: 06.05.2025
• Expiry Date: 20.06.2025

The Regulatory Affairs Manager oversees the regulation process for medical devices and products requiring governmental approval. Responsibilities include preparing applications, handling government interactions, supporting strategic regulatory planning, coordinating inspections, and developing compliance procedures for pre- and post-market activities.

Key responsibilities include:

1. Implementing regulatory strategies for Medical Devices via national and international procedures.
2. Assisting in the creation and updating of Technical Files.
3. Managing clinical investigations and reviewing related documentation.
4. Overseeing post-marketing surveillance activities.
5. Supervising international regulatory and quality assurance activities.

• Master’s Degree in science or a related field; MD is a plus.
• Extensive experience in life sciences and Regulatory Affairs.
• Proficiency in English and Italian; additional languages are a plus.
• Proficient in Microsoft Office.
• Excellent communication, planning, and organizational skills.
• Ability to handle multiple priorities effectively.