Valerie Laffineur is an experienced professional with extensive expertise in quality control and analytical development within the pharmaceutical industry. Currently serving as a QC Non-Routine Laboratory Manager at Viatris since July 2019, Valerie oversees a team of 10, responsible for the introduction and successful transfer of new products, including solid forms and stability studies. As Quality Control Manager at ERYTECH Pharma since January 2016, Valerie manages the quality control of raw materials and medical devices for sterile blood products, while also overseeing a controlled atmosphere area and conducting regulatory stability studies. Valerie's previous roles include Senior Consultant at CVO-EUROPE, Analytical Development Manager at Theramex-TEVA, and various analytical chemistry positions at Afssaps and Ethypharm, demonstrating a strong foundation in laboratory management and method development. Valerie holds a Master II degree in Physico-Chemistry of API and has an undergraduate degree in chemistry from Université de Montpellier.
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