Qserve Group is pleased to announce that François Naye has joined our team to further expand his capabilities in supporting the medical device industries worldwide.
François Naye has joined the Qserve Group where he is part of the Qserve Conseil team and experienced in developments particular in software. François holds a PhD in molecular biology from the university of Bordeaux. He worked 5 years as a researcher in Belgium universities prior jumping into the quality and regulatory affairs world. He worked two years for a small IVD company where he was in charge of establishing technical documentation and risk management activities for certified products under the medical device directive.
François joined an international Belgian medical device company where he learned to work in multicultural environment. This experience provides him an interest into the management of software. One of the reasons for which he joined for 3 years a medical device startup working on sleep apnea. He has implemented a quality management system and the technical documentation for European and US regulations. In the last position as Quality Manager, François can now offer his calmness, pragmatism and professionalism as a consultant.
In all his different positions, François has sought to be involved in training activities as he finds it rewarding to make people aware and autonomous. With his scientific knowledge, his quality and regulatory experience and his passion for innovation, François wants to help companies to make their product available to improve patient’s life.
About Qserve Group
Qserve’s mission is to support all medical device and in-vitro diagnostics manufacturers with a practical approach, translating existing regulations to understandable requirements. We serve to guide manufacturers in gaining and maintaining compliance as well as conducting clinical studies as a CRO to ensure safe and quality devices in the most streamlined way possible. Qserve’s global team combines its regulatory and clinical knowledge and experience in the medical device industry, sharing more than 900 years’ worth of combined expertise in the medical field. Having teams in the EU, USA, and China provides a global footprint for global regulatory, clinical, CRO and quality services.
Qserve is constantly looking for consultants at different career levels with experience in regulatory affairs, quality assurance, clinical affairs or auditing in medical devices. Check our current vacancies