Natasha Rivas has more than 20 years of experience in the pharmaceutical and medical device industry, including 15 years working in the CDMO space. Natasha was previously the VP of Quality at SCA Pharmaceuticals and Director of Quality Assurance and Quality Control at Vetter Pharma’s clinical manufacturing site in Chicago, IL. Prior to this, she held roles of increasing responsibility in quality control, quality assurance, and regulatory affairs at Abbott Laboratories and Hospira. She leads the design, implementation, and iteration of the quality systems and processes that meet customers’ evolving needs and ensures delivery of safe and effective products at Genezen.
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