Jessica Sabol
About Jessica Sabol
Jessica Sabol is a Quality Assurance Documentation Lead at Kite Pharma, where she has worked since 2021. She has extensive experience in quality assurance and validation, having held various roles in companies such as Penn Medicine, ProPharma Group, and Bristol-Myers Squibb.
Current Role at Kite Pharma
Jessica Sabol serves as the Quality Assurance Documentation Lead at Kite Pharma since 2021. In this role, she is responsible for overseeing documentation processes related to quality assurance. Her expertise contributes to maintaining compliance with industry standards and regulations in the biopharmaceutical sector.
Previous Experience in Quality Assurance
Prior to her current position, Jessica Sabol held various roles in quality assurance and validation. She worked at Kite Pharma as a Quality Assurance Documentation Specialist from 2020 to 2021. Additionally, she served as a Validation Specialist at ProPharma Group in 2017 and as a Quality Systems Validation Specialist at Penn Medicine from 2013 to 2014.
Educational Background
Jessica Sabol is pursuing a degree in Liberal and Professional Studies at the University of Pennsylvania, a program she has been engaged in since 2014. She holds a Bachelor's Degree in Biology/Biological Sciences from Frostburg State University, where she studied from 2009 to 2012. Her educational background supports her work in the life sciences and quality assurance fields.
Career History
Jessica Sabol has a diverse career history in the life sciences and quality assurance sectors. Her experience includes roles at notable companies such as Bristol-Myers Squibb, where she worked as a Document Specialist, and Lonza, where she held positions including Supervisor, Technical Operations and Quality Records Project Manager II. She also worked at Godiva Chocolatier as an Assistant Manager early in her career.
Early Career and Education
Jessica Sabol began her professional journey after completing her high school education at Glenelg High School from 2005 to 2009. She gained initial experience as a Temp at Key Technologies in 2012. Her early career included a position as a Validation Scientist at cGMP Validation LLC, where she worked for a month in 2013.