Madeleine Melchior
About Madeleine Melchior
Madeleine Melchior is a Senior Manager in Regulatory Affairs and Team Lead for New Markets EMEA at BeiGene, based in Basel, Switzerland. She has extensive experience in regulatory affairs across pharmaceutical and nutraceutical sectors, having worked at companies such as Nestle Skin Health/Galderma, Bayer, and Actavis.
Current Role at BeiGene
Madeleine Melchior is currently serving as the Senior Manager of Regulatory Affairs and Team Lead for New Markets in the EMEA region at BeiGene, based in Basel, Switzerland. In this capacity, she leads the regulatory strategy for launching new pharmaceutical products in emerging markets within the EMEA region. Her role involves managing regulatory frameworks to ensure compliance with local and international standards.
Previous Experience at Nestle Skin Health/Galderma
Madeleine Melchior worked at Nestle Skin Health/Galderma in several roles between 2015 and 2019. She started as a Regulatory Affairs Project Manager Nutraceuticals in Egerkingen, Switzerland, and then advanced to Global Regulatory Affairs Manager before taking on the role of Senior Global Regulatory Affairs Manager in La Tour de Peilz, Switzerland. She played a key role in obtaining market authorizations for biotech products and contributed to the regulatory approval of high-profile dermatological products.
Educational Background
Madeleine Melchior holds a Master of Science in Pharmacy from Uppsala University, where she studied from 2006 to 2011. She also holds a Master's degree from the University of Sydney, which she completed in 2010. Additionally, she studied at Röda Korsets Folkhögskola (The Red Cross University College Sweden) for one year, working towards a Bachelor's degree.
Industry Experience and Skills
With extensive experience in the pharmaceutical and nutraceutical sectors, Madeleine Melchior has held various roles in regulatory affairs at notable companies, including Bayer and Actavis. Throughout her career, she has specialized in navigating complex regulatory environments to expedite product approvals. Her expertise includes managing cross-functional teams, developing and implementing regulatory frameworks, and mentoring junior professionals.
Role in Regulatory Affairs
Madeleine Melchior has a robust background in regulatory affairs, specializing in both pharmaceutical and nutraceutical products. She has led teams to achieve significant regulatory milestones and has developed and implemented regulatory strategies to facilitate the approval of products. Her extensive experience includes working on market authorizations for biotech products and ensuring compliance with local and international standards.