Ludivine Lopez
About Ludivine Lopez
Ludivine Lopez is a professional specializing in qualification and validation processes, currently serving as the team leader at Laboratoire Aguettant since 2018. She has extensive experience in the pharmaceutical industry, having held various roles at notable companies such as BD, Merck Sharp & Dohme, and Sanofi Pasteur.
Current Role at Laboratoire Aguettant
Ludivine Lopez serves as the Responsable équipe Qualification / Validation at Laboratoire Aguettant. She has held this position since 2018, contributing to the company's efforts in ensuring compliance and quality in product development and validation processes. Her role involves overseeing a team dedicated to qualification and validation activities, which are critical in maintaining the integrity of laboratory operations.
Previous Experience at BD
Ludivine Lopez has extensive experience at BD, where she worked in various capacities. She served as a Consultante CVO-EUROPE, focusing on process validation from 2011 to 2012. Additionally, she held roles as a Consultante CVO, managing industrialization and validation projects from 2015 to 2017, and as a technical coordinator for product and process validation from 2013 to 2014. Her time at BD provided her with a solid foundation in quality assurance and process engineering.
Educational Background
Ludivine Lopez studied at the Institut national des Sciences appliquées de Rouen, where she earned an INSA Engineer degree in Chemistry & Process from 2006 to 2009. Prior to this, she attended Lycée Joffre - CPGE from 2004 to 2006, completing a two-year program that prepared her for advanced studies in engineering.
Experience at Sanofi Pasteur and Merck
Ludivine Lopez has worked at Sanofi Pasteur as a CVO-EUROPE Contractor, focusing on QC lab equipment qualification for three months in 2011. She also gained experience at Merck Sharp & Dohme as a CVO-EUROPE Contractor, where she worked as a Process Engineer for ten months in 2010. Her roles at these organizations contributed to her expertise in quality control and process validation.
Consulting Experience with CVO-EUROPE
Ludivine Lopez worked as a Consultant at CVO-EUROPE from 2010 to 2017. During this seven-year period, she was involved in various projects related to process validation and quality assurance. Her consulting experience allowed her to develop a broad understanding of industry standards and practices in the pharmaceutical and biotechnology sectors.