Beth Zito possesses extensive experience in analytical development and quality control within the pharmaceutical industry, having held various positions at Gilead Sciences from 2010 to 2018. As a Quality Control Chemist III at Gilead Sciences Ireland UC, Beth contributed to the finalization of clinical batches and led bioavailability studies supporting NDA filings. Prior roles included Research Associate in both Analytical Development and Formulations, where responsibilities encompassed conducting dissolution experiments, performing analytical techniques such as HPLC and UPLC, and training peers. Recognized for significant contributions, Beth received multiple awards, including a Values at Work Award. Beth holds a Bachelor of Arts in Chemistry with a minor in Justice Studies from San José State University.
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