Rosa Khelifa
About Rosa Khelifa
Rosa Khelifa is a Senior Regulatory Affairs Officer at Laboratoire Aguettant, with extensive experience in regulatory activities related to vaccines. She previously worked at Sanofi Pasteur for several years in various roles, focusing on regulatory CMC activities and global regulatory intelligence.
Work at Laboratoire Aguettant
Rosa Khelifa has been employed at Laboratoire Aguettant as a Senior Regulatory Affairs Officer since 2017. In this role, she is responsible for overseeing regulatory compliance and ensuring that products meet necessary legal standards. Her work contributes to the company's ability to navigate complex regulatory environments effectively.
Experience at Sanofi Pasteur
Prior to her current position, Rosa Khelifa worked at Sanofi Pasteur for a total of five years from 2012 to 2017. During this time, she held various roles including Regulatory CMC consultant, where she coordinated CMC activities for vaccine registration and managed regulatory registration and maintenance activities. She also served as a Coordinator for global regulatory activities, focusing on regulatory intelligence and processes.
Educational Background
Rosa Khelifa studied at the Faculty of Pharmacy of Montpellier, where she achieved her Pharmacist graduation from 2003 to 2008. She furthered her education by studying Production Engineering and Project Management, obtaining a Master 2 degree from 2009 to 2010. This educational background has equipped her with the knowledge necessary for her roles in regulatory affairs.
Regulatory Affairs Expertise
With extensive experience in regulatory affairs, Rosa Khelifa specializes in CMC activities related to vaccines and serum. Her expertise encompasses regulatory registration, maintenance activities, and compliance with global regulatory standards. This specialization is critical in ensuring that pharmaceutical products are developed and marketed in accordance with regulatory requirements.