Stephane Turcat
About Stephane Turcat
Stephane Turcat is an International Regulatory Affairs Director with over 20 years of experience in regulatory affairs and sciences, currently working at UPSA and Bristol-Myers Squibb in Paris, Île-de-France, France.
Current Roles in Paris, Île-de-France
Stephane Turcat is currently serving as the International Regulatory Affairs Director at Bristol-Myers Squibb in Paris, Île-de-France, France. Concurrently, he holds the position of International Regulatory Sciences Director at UPSA in the same region. In these roles, Turcat oversees the regulatory affairs and sciences teams, ensuring compliance with international standards and driving the successful approval of pharmaceutical products.
Previous Experience at Servier
From 1996 to 2000, Stephane Turcat worked as a Project Leader at Servier. During his tenure, he led multiple international regulatory projects, contributing significantly to the company's global market reach. His efforts in these projects were aimed at navigating the complex regulatory landscape, ensuring that Servier's products met the necessary compliance standards across various international markets.
Consultancy and Management at Laboratoires Expanscience
Stephane Turcat served as a Senior Consultant at Laboratoires Expanscience from 2013 to 2015. Here, he focused on regulatory strategies primarily for dermatological products. His role involved advising on strategic regulatory planning and ensuring the successful navigation through the regulatory processes for product approvals.
Regulatory Roles at Amgen and Merck
At Amgen, from 2007 to 2010, Stephane Turcat worked as a Regulatory Affairs Senior Manager and Consultant. During his tenure, he contributed to the successful regulatory approval of several biologic products. Prior to that, from 2002 to 2007, he served as a Regulatory Affairs Manager at Merck, playing a key role in the regulatory submissions for cardiovascular and diabetes medications. His contributions were critical in ensuring these products met all necessary regulatory requirements.
Early Career and Education
Stephane Turcat began his career in regulatory affairs at Sanofi in 2001, where he was involved in the regulatory processes for a major vaccine project. He holds a doctorate in pharmacy, achieved from 1986 to 1993. Additionally, he studied at Chatrapati Sahuji Maharaj Kanpur University from 1996 to 1999. With over 20 years of experience in regulatory affairs and sciences, Turcat brings a wealth of knowledge and expertise to his current roles.