Camille de Durand

WORK HISTORY

EDUCATION

ABOUT CAMILLE DE DURAND

I’m currently working as a EU Regulatory Affairs Project Manager at Panpharma, where I contribute to the management of regulatory submissions and lifecycle activities across Europe, UK, Palestine and Israel. My role allows me to combine technical rigor with project coordination, ensuring compliance and the continuous availability of high-quality medicines.Graduated as an Engineer in Industrial Biology (EBI – École de Biologie Industrielle) and holder of a Master’s degree in Technical and Regulatory Affairs (IPIL Lyon / emlyon business school), I’ve built a strong foundation in regulatory science, CMC documentation, and European pharmaceutical legislation.Over the past few years, I’ve developed a genuine interest in how regulation supports innovation and patient access. Beyond pharmaceuticals, I’m particularly drawn to the fields of nutrition, preventive health and wellness, where science can make a tangible impact on daily life.As a triathlon and endurance sports enthusiast, I’m personally engaged in the pursuit of balance, performance and health. This mindset influences the way I work : with perseverance, discipline and curiosity.Certified Lean Six Sigma Green Belt, I use structured and pragmatic approaches to improve processes, strengthen quality, and encourage collaboration across teams.I’m motivated by opportunities where science and regulation meet purpose, contributing to a more accessible and innovative vision of health.