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 began her carreer in IVD MD at the international company BIO-RAD as an R1D 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 strat-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 stratup and continuing to CARMAT (project quality consultant). 

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

She has 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