REGULATORY AFFAIRS SPECIALIST

Orienta Orienta Spa - Benefit Society, Verona branch, is selecting a REGULATORY AFFAIRS SPECIALIST for their client in the metalmechanical sector at their headquarters located in Villafranca di Verona. For almost forty years, the company has been involved in designing and producing orthopedic products, seeking modern technologies and innovative solutions for human well-being. The inserted resource will be dedicated to the following tasks: - Development and management of technical files for medical devices, in accordance with MDR (Regulation (EU) 2017/745); - Management of regulatory compliance according to European MDR; - Supervision of CE marking and management of regulatory registrations. REQUIREMENTS - Bachelor's degree in biomedical engineering; - Previous experience in regulatory roles; - In-depth knowledge of MDR for medical devices; - Ability to write and develop technical files conforming to MDR; Completing the profile - Teamwork attitude; - Good problem-solving skills; - Seriousness and punctuality - proactive approach to the task Initial contract in fixed-term employment with possibility of continuing the employment relationship. Insertion with CCNL Metalmechanics Small Industry CONFIMI. 13 months. Full-time working hours: 40 hours from Monday to Friday, from 8 am to 12 pm and from 1 pm to 5 pm. Work zone: Villafranca di Verona. Sector: Metalmechanical industry Role: Other Manages other people: No Type of occupation: Temporary work for the purpose of hiring