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Deb Pendola has over 20 years of work experience in the pharmaceutical industry. Deb started their career as a Regulatory Operations Associate at Biogen in 2001, where they were responsible for various regulatory tasks. In 2005, they joined Shire as a Senior Regulatory Operations Specialist, where they managed the compilation and publication of regulatory submissions. At Shire, Deb also collaborated with global regulatory affairs staff to ensure compliance with technical and format requirements. In 2010, Deb moved to Fresenius Medical Care North America as a Sr. Regulatory Publishing Specialist. In this role, they tracked, processed, and published regulatory submissions in accordance with FDA regulations and internal requirements. Deb also served as a technical leader for eCTD submissions and managed electronic archives and repositories. Deb's most recent position was as a Senior Manager of RA Operations Publishing at Celldex Therapeutics, where they oversaw publishing operations in regulatory affairs.

Deb Pendola holds a Bachelor of Science (B.S.) degree in Business Administration and Management, with a focus on General studies, from New Hampshire College. The specific years of their education were not provided.