Karin Schaedel is an experienced Regulatory Affairs Manager at Getinge since November 2025, specializing in compliance and regulatory matters within the medical technology sector. Previously, Karin served as a Consultant QA/RA at Plantvision AB from September 2022 to November 2025, where responsibilities included monitoring regulations and conducting impact assessments. Karin completed a Master Thesis at KTH Royal Institute of Technology, focusing on modeling dilution effects in pediatric intravenous drug treatments to minimize medication errors. Prior to these roles, Karin worked as a Healthcare Administrator at Doktor.Se and Kry, managing patient communications and Covid-19 testing logistics. Karin holds a Civilingenjörsexamen in Medical Technology and Physics from KTH Royal Institute of Technology, with additional educational experience at Lund University.
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