Esperto per Certificazione dispositivi medici

The role of Esperto per Certificazione dispositivi medici at Eurofins involves joining an internationally recognized leader in laboratory services, offering expert support for the certification and compliance of medical devices. The selected candidate will be part of a specialized team responsible for ensuring that medical devices meet regulatory and quality standards required for market approval across Europe and globally. The team collaborates closely with regulatory bodies and manufacturers, serving as trusted advisors throughout the certification process.

Key responsibilities include evaluating documentation and conducting technical reviews to assess compliance with medical device regulations such as the MDR (Medical Device Regulation) and related standards. The expert will coordinate certification activities, interact with clients to clarify regulatory requirements, and provide guidance on corrective actions necessary for approval. Day-to-day tasks involve reviewing technical files, preparing compliance reports, and supporting external and internal audits.

The ideal candidate will have an advanced degree in biomedical engineering, engineering, life sciences, or related fields, along with several years of professional experience in medical device certification or regulatory affairs. Strong knowledge of European and international medical device regulations, particularly MDR, is essential. Excellent analytical skills, attention to detail, and proficiency in both written and spoken Italian and English are required, while experience with quality management systems such as ISO 13485 is highly valued.

Eurofins offers competitive compensation and a comprehensive benefits package, including professional development opportunities, flexible working conditions, and a dynamic, international work environment. Employees are encouraged to pursue continuous learning and growth within a global network of experts.