Erik Olsson

Erik Olsson is a Regulatory Affairs Specialist at Neoventa Medical since August 2023, with a strong background in quality assurance and regulatory affairs in the medical device industry. Previously, Erik served as QARA Manager at Cuviva AB, where responsibilities included compliance assurance with medical device regulations. Erik has also held positions as RA Manager at Wellspect HealthCare, ensuring compliance and registrations, and as a Senior Consultant at Knightec, focusing on medical device software development. Earlier roles include consulting at Semcon for data management systems and assisting in research projects at Chalmers University of Technology, where Erik contributed to healthcare innovation. Erik holds a Master of Science in Industrial Engineering and Management from Chalmers University of Technology and a Bachelor of Science in Mechanical Engineering from Jönköping University.