Luis Vaz is an Associate Regulatory Affairs Director at AstraZeneca, bringing over 25 years of global regulatory affairs experience. Previously, they served as a Freelance Regulatory Consultant for GlaxoSmithKline and as a Senior Regulatory Affairs Associate at Allergan, where they managed submissions for multiple markets. With a strong educational background in chemistry, including a Diplome d'Ingenieur and an MSc in Organic Chemistry, Luis has demonstrated expertise in managing complex regulatory submissions and compliance across diverse international markets. Additionally, they have held various roles at AstraZeneca, contributing to the successful project management of drug submissions and lifecycle activities across numerous emerging markets.
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