Marion Schimpgen

Marion Schimpgen is a seasoned professional in regulatory affairs with extensive experience in the pharmaceutical and chemical industries. Currently serving as a Technical Regulatory Affairs Manager at Roche since November 2014, Marion is responsible for managing high-quality regulatory submissions for technical changes, renewals, and clinical trial applications globally, while collaborating with various internal stakeholders and corporate partners. Prior roles include Regulatory Affairs Document Specialist at Roche, where Marion prepared and managed regulatory documents, and positions at DC DruckChemie GmbH, where responsibilities ranged from product development and quality control to technical support and customer consultation. Marion holds a Master's degree in Forensic Science and Technology and a Bachelor of Science in Applied Sciences and Forensic Investigation from Teesside University, complemented by a University Diploma of Technology in Chemistry from Université Robert Schuman.