Nitto Avecia
Danielle Santello is a seasoned quality assurance professional with extensive experience in the pharmaceutical and biotechnology industries. Currently serving as Quality Assurance Manager at Nitto Avecia since October 2022, Danielle leads trend analysis data collection and acts as the lead auditor for vendor and internal quality audits, ensuring cGMP compliance. Previous roles include Quality Assurance Senior Consultant at American Pharmaceutical Consulting, Quality Manager at Sanofi, and various positions at Genzyme and AstraZeneca, where responsibilities ranged from managing quality oversight in contract manufacturing to coordinating QC workflows and compliance with regulatory requirements. Danielle holds a BA in Biology with minors in Chemistry and Communication from Rhode Island College, and a Certificate of Professional Achievement from Northeastern University.
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Nitto Avecia
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Oligonucleotides are giving rise to a new generation of therapeutics—and Nitto Avecia is helping lead the way. With more than 25 years’ experience in oligonucleotide development and production, we are the partner of choice for pharmaceutical innovators creating new drugs with the power to transform treatment for a wide range of diseases. In partnership with Nitto Avecia Pharma Services, Nitto Avecia is the first CMO that offers a comprehensive, end-to-end oligonucleotide solution. This offers the advantage of a single, expert partner handling the entire process—from drug substance through drug product manufacturing—with flexible solutions and consistent reliability and quality.