Nethe Eva Touborg Bune

Nethe Eva Touborg Bune is a seasoned professional in regulatory affairs, currently serving as a Senior Regulatory Affairs Specialist at Bavarian Nordic since October 2020, focusing on CMC and tech transfer activities for marketed biologics. Prior experience includes roles at Ambu A/S as a Regional RA/QA specialist and extensive positions at Novo Nordisk, where responsibilities encompassed the development and approval of Software as a Medical Device, management of CMC and device lifecycle activities, and compliance oversight. Nethe's academic background includes a Master of Science in Parasitology and various regulatory affairs modules from the University of Copenhagen, alongside a Bachelor's degree in Medical Laboratory Science. Additional experience encompasses research and laboratory roles in medical science and public health.