ÂÜÀòÂÒÂ×

Camille Ribolzi has worked in a variety of roles in the biomedical engineering field since 2013. Her first role was as a R&D Engineer (internship) at ICET Lab in 2013. Camille then worked as a Regulatory Affairs Engineer (internship) at FCI Ophthalmics, followed by a role as a R&D Engineer (university company) at Biotika®. In 2013, they were also a Stagiaire ingénieur biomédical at Nouvel Hôpital Civil. In 2014, they worked as a Clinical Engineer at Materialise, followed by a Quality Engineer (internship) at DEFYMED. In 2017, they were a R&D Biomedical Engineer at PDR International Centre for Design and Research. From 2018 to 2021, they were the Head of cranio maxillofacial department - Senior biomedical engineer at 3D LifePrints. Most recently, they have been the Quality and Regulatory Affairs Manager at INBRAIN Neuroelectronics, where they set up and implemented the Quality Management System according to ISO 13485:2016, for development and manufacturing of class III medical devices. Camille also successfully led and executed the transfer of the Quality Management System from SharePoint to a digital Quality Management System, and entirely customized the eQMS solution to the company's needs.

Camille Ribolzi completed their BAC S in 2008 at Lycée Ribeaupierre in Ribeauvillé, 68, with an option in SVT. From 2008 to 2010, they attended Lycée Henry Poincaré in Nancy for Classes préparatoires Biologie Chimie Physique Sciences de la Vie et de la Terre (BCPST). From 2011 to 2014, they studied Ingénierie biomédicale/médicale at ISIFC.