Regulatory Affairs Sustaining Specialist
EnovisFriuli – Venezia Giulia, Italy
Posted November 12, 2025
Full Time
About the Company
Enovis is a global innovation-driven company in the medical technology sector, committed to improving patients' quality of life.
Job Description
We are seeking 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)
Benefits
- equal employment opportunities to all individuals
- policy of equal treatment for all employees and applicants
