Céline Rigaudeau
About Céline Rigaudeau
Céline Rigaudeau is a regulatory affairs manager with extensive experience in the pharmaceutical industry, currently serving as Responsable Affaires Réglementaires - Zone Export at Laboratoire Aguettant since 2019. She has over a decade of management experience and has worked in various regulatory roles, including significant positions at Boiron and Umanis.
Current Role at Laboratoire Aguettant
Céline Rigaudeau currently serves as Responsable Affaires Réglementaires - Zone Export at Laboratoire Aguettant. She has held this position since 2019, contributing to the regulatory affairs department in the Région de Lyon, France. In her role, she specializes in drafting variation request dossiers specifically for injectable medications, ensuring compliance with regulatory standards for pharmaceutical products.
Previous Experience in Regulatory Affairs
Prior to her current position, Céline Rigaudeau worked at Umanis as Senior Regulatory Affairs Manager from 2013 to 2019. Her earlier experience includes a role as Consultante Affaires Réglementaires at Consultys for four months in 2013. Additionally, she served as Directrice adjointe Affaires Règlementaires at Boiron from 2001 to 2012, where she gained over a decade of management experience in regulatory affairs.
Educational Background in Pharmacy
Céline Rigaudeau studied at the Faculté de Pharmacie Paris V, where she earned her Docteur en Pharmacie from 1995 to 2001. She also pursued further education at IPIL / EM Lyon, achieving a Master II in Pharmacie Industrielle with a focus on Affaires Technico-Règlementaires from 2000 to 2001. This educational foundation supports her expertise in regulatory affairs.
Expertise in Regulatory Affairs
Céline Rigaudeau possesses extensive experience in regulatory affairs, covering both human and veterinary products. Her expertise includes working with generics, vaccines, homeopathic and phytotherapeutic medicines, cosmetics, and dietary supplements. This diverse knowledge base enables her to navigate complex regulatory environments effectively.