Carine Schadeck
About Carine Schadeck
Carine Schadeck is a Regulatory Manager with over 25 years of experience in regulatory affairs and clinical supply operations, currently working at Bristol-myers Squibb and Thrombogenics.
Title
Carine Schadeck holds the position of Regulatory Manager, serving in leading pharmaceutical companies in Europe and the United States, with a specialization in regulatory affairs and clinical supply operations.
Company
Carine Schadeck is currently employed at Bristol-myers Squibb in New Jersey, United States, and Thrombogenics in Leuven, Vlaams-brabant, Belgium, where she holds managerial roles in regulatory affairs. She has also worked at Pfizer, and Bristol-myers Squibb International Corp in various regulatory and supply chain management capacities.
Education and Expertise
Carine Schadeck earned a master's degree in Nutrition from Université Catholique De Louvain. With over 25 years in the field, she is well-versed in European and American regulatory environments, focusing on vaccines and major pharmaceutical products.
Background
Carine Schadeck has extensive experience in regulatory affairs and clinical supply chain management. She began her career at Bristol-myers Squibb International Corp as a Clinical Supply Coordinator (1996-2000) before moving up to Senior EU Regulatory Coordinator (2000-2006). She then joined Pfizer, serving as a Regulatory Affairs Associate (2006-2008) and later as Global Regulatory Affairs Manager for Vaccines (2008-2010). She now manages regulatory affairs at Bristol-myers Squibb and Thrombogenics.
Achievements
Throughout her career, Carine Schadeck has played a pivotal role in managing regulatory submissions and approvals for significant pharmaceutical products. Her work on global regulatory strategies for vaccines during her tenure at Pfizer is a notable highlight. Her substantial expertise in clinical supply chain management and global distribution has contributed to her well-regarded status in the industry.