Regulatory Affairs Sustaining Specialist

We are looking for an experienced Regulatory Affairs Sustaining Specialist to join our Regulatory Affairs department, with a background in the medical device industry. The ideal candidate has a scientific education and will be responsible for preparing and managing technical documentation to maintain medical device certifications in compliance with MDR regulations.

Requirements

• Degree in scientific disciplines (Biology, Chemistry, Biomedical Engineering, or related fields)
• At least 1–2 years of experience in Regulatory Affairs within the medical device industry
• Knowledge of MDR and major international regulations applicable to medical devices
• Good time and priority management skills
• Excellent command of Italian and English (B2/C1 level)
• Proficiency in Microsoft Office, especially Excel
• Accuracy, methodical approach, and results orientation
• Strong interpersonal skills and ability to work in multicultural teams
• Willingness to learn and collaborate
• Availability for short business trips to Switzerland (2–3 days per quarter) is required