Emilie Fournier, PhD

Emilie Fournier, PhD has been working in the medical device industry since 2011. Emilie began their career at FIRALIS SAS as a R&D Project Manager - Biomarker Products, where they were responsible for the development of ELISA kits to detect cardiovascular biomarkers in patient samples. Emilie then moved to Roche in 2014, where they held two roles: Manufacturing Science and Technology Engineer and Project Manager. In their role as Manufacturing Science and Technology Engineer, they provided technical and scientific support of downstream processing operations, statistical and data analysis support for troubleshooting activities and various projects, and process monitoring using statistical process control (SPC). As Project Manager, they were responsible for multi-project management with international partners, implementation of project-management tools, and implementation of risk-management tools. In 2016, they joined ISOCELE CONSEIL as a Consultant RA/QA for the Medical Device industry. Currently, they are working at both dianosic and Airel-Quetin as a PRRC - QA/RA and Quality/Regulatory coordinator, respectively.

Emilie Fournier holds a Lead Auditor ISO 13485 IRCA certification from BSI Training Academy, which they are currently pursuing. Emilie has a PhD in Biochemistry from the University of Strasbourg, which they obtained in 2010. Emilie also holds a Master in Molecular Biology and Virology from Université Henri Poincaré, Nancy 1, which they obtained in 2005. Additionally, they are currently pursuing a certification from BSI Training Academy in MDR 2017/745.