Validant
Aida Sio is an experienced quality control professional with a strong background in the biopharmaceutical industry. Currently serving as the Director of Quality Control at MaSTherCell, Aida oversees various functions including Analytical Development and Microbiology for gene therapy products. Aida also works as a Senior Consultant for Black Diamond Networks, focusing on CMC document preparation and review, and holds the position of Interim QC Manager of Raw Material at Validant, where responsibilities include establishing a new laboratory and developing necessary SOPs. Previous roles include QC Senior Manager for Viral-based Therapeutics at Lonza and Consultant at Validant, along with significant experience in regulatory submissions and laboratory operations management at Cardinal Health and Arena Pharmaceuticals. Aida Sio holds a Bachelor of Science in Chemistry from the University of the Philippines and a Master's degree in Chemistry from the University of New Orleans.
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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?