Sébastien Renard
About Sébastien Renard
Sébastien Renard serves as the Directeur de l'Agence de Meaux, a position he has held since 2021. He has extensive experience in regulatory affairs and quality assurance, having worked for various medical companies in France over the past two decades.
Current Role at Petits-fils
Sébastien Renard serves as the Directeur de l'Agence de Meaux at Petits-fils since 2021. In this role, he oversees operations and management within the agency located in Meaux, Île-de-France, France. His responsibilities include ensuring the quality of services provided and maintaining the standards expected by clients and stakeholders.
Previous Experience in Regulatory Affairs
Sébastien Renard has extensive experience in regulatory affairs across various organizations. He worked at Covidien (Medtronic Minimally Invasive Therapies Group) as the Director of Regulatory Affairs from 2013 to 2017. Prior to that, he held the position of Director of Regulatory Affairs at Terumo Europe from 2010 to 2013. His role involved managing compliance and regulatory strategies within the medical device sector.
Quality Assurance Background
Sébastien Renard's career includes significant roles in quality assurance. He was the Quality Assurance Manager at Corneal Industrie SAS from 1999 to 2001. He later served as the Quality Assurance and Regulatory Affairs Manager EMEA at Biosphere Medical, SA from 2001 to 2006, and at Hillrom from 2006 to 2010. These positions focused on maintaining quality standards and regulatory compliance in the medical field.
Regulatory Affairs Management at Medtronic
From 2018 to 2021, Sébastien Renard worked at Medtronic as a Senior Regulatory Affairs Manager EMEA. In this capacity, he was responsible for overseeing regulatory processes and ensuring that products met the necessary compliance requirements across the European market. His experience in this role contributed to his expertise in navigating complex regulatory landscapes.