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Genezen Appoints Natasha Rivas as VP of Quality Assurance and Regulatory Affairs

Rivas brings more than 20 years of experience in the pharmaceutical and medical device industry.

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By: Charlie Sternberg

Associate Editor

Genezen Inc., a cell and gene therapy Contract Development and Manufacturing Organization (CDMO), has appointed Natasha Rivas as vice president of Quality Assurance and Regulatory Affairs.   Rivas will be responsible for the design, implementation and iteration of the quality systems and processes that meet customers’ evolving needs and ensure delivery of safe and effective drug products.   Rivas brings more than 20 years of experience in the pharmaceutical and medical device industry, previousl...

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