Validant
José Zorrilla, MS, is an experienced quality professional with a robust background in the pharmaceutical and biotechnology industries. Currently serving as a Quality Consultant at Intas Pharmaceuticals and as Quality Assurance Lead at MassBiologics, José has previously held significant roles such as Quality Systems Lead at Novavax and Quality Consultant at Shanghai ZhenGe Biotech Co., Ltd. As Head of Quality at Sanofi Pasteur, José was responsible for the quality strategies supporting COVID-19 vaccine production and oversaw commercial vaccine quality at multiple sites. Notably, José held the position of Director of Quality Assurance at Eli Lilly and Company for over two decades, where responsibilities included driving quality systems improvements, ensuring compliance, and leading strategic initiatives. José holds a Master of Science in Cell and Molecular Biology from Boston University and a Bachelor of Science in Biology from Iowa State University.
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Validant
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Validant is a full-service life science consulting firm serving developers and manufacturers of pharmaceuticals, biologics, medical devices, and diagnostics worldwide. We partner with these companies to ensure safe and reliable access to life-saving healthcare products, facilitating their efficient, compliant progression from preclinical and clinical phases through to manufacturing and distribution—and optimizing quality at each step. Our platform brings together leading specialists in each facet of the product lifecycle, and we have curated an extensive and diverse global network of consultants to help execute strategies worldwide. Because of this, Validant is able to deliver our breadth of consulting, execution, and support services in the right place, at the right level, and in the right combination to meet your exact need. We've empowered hundreds of clients – from start-ups to the largest global leaders – to efficiently navigate regulatory, compliance, and quality complexities. How can we help you?