Senior Consultant in Quality and Regulatory Affairs for medical devices

MSc in Research and Innovation with a specialization in in vitro diagnostic medical devices (IVD MD) from University of Angers (ISSBA)
MSc in Quality and Health Products with a specialization in medical devices (MD) from University of Paris Sud

Camille has began her carreer in IVD MD at the international company BIO-RAD as an R&D project manager involved in product development, validation, feasibility and stabilities studies. After this first experience, she started to deep dive on quality by joining the French pharmaceutical laboratory GERBET as a quality apprentice in the clinical development department. 

Following this experience, she integrated the consulting field by joining CADUCEUM. For 4 years, she accompanied and advised clients on regulatory affairs and quality both in start-ups and big companies. More specifically, she carried out her main missions at BECKTON DICKINSON (Quality Project consultant) then as quality and regulatory affairs manager within a start-up and continuing to CARMAT (project quality consultant). 

She has then pursued her career at the French Pharmaceutical Laboratory CCD for 3 years as MD product quality manager. 

She has acquired a solid experience in project management, quality management (NC/CAPA management, creation of procedures, preparation of audits), regulatory affairs (creation/updating of technical files), design until a medical device is marketed. And also complaint management, medical device vigilance, validation of advertising materials, post-market surveillance and the release of sterile medical devices. 

She joined ATESSIA in November 2022 as a quality and regulatory affairs consultant to develop new Business Unit “Medical Devices”. 


Medical devices

Product & System
Quality Management

Regulatory Strategy