Sang Jeon
About Sang Jeon
Sang Jeon is a Sr. Scientist Investigator at Bristol Myers Squibb with extensive experience in bio therapeutics and a background in quality control and cell processing.
Current Position at Bristol Myers Squibb
Sang Jeon currently holds the position of Sr. Scientist Investigator at Bristol Myers Squibb. He is based in Summit, New Jersey, United States. In this role, he is involved in developing and improving biotherapeutic processes and carries out investigations that are crucial to the advancement of medical research and patient care.
Previous Role at Legend Biotech
From 2020 to 2021, Sang Jeon worked as a QC Investigator at Legend Biotech in Raritan, New Jersey, United States. During his one-year tenure, he contributed to quality control processes, ensuring that biotechnological products met rigorous standards both in development and production stages.
Experience at Novartis
Sang Jeon had a substantial career at Novartis, where he served as a QC Scientist from 2017 to 2020 and as a Sr. Cell Process Specialist from 2013 to 2017. Based in Morris Plains, NJ, he spent a total of seven years at the company. His roles focused on cell processing and quality control, crucial for maintaining the reliability and effectiveness of biotherapeutic products.
Early Career at Dendreon
From 2011 to 2013, Sang Jeon worked as a Cell Processing Associate at Dendreon in Morris Plains, NJ. Over his two-year tenure, he contributed to the cell processing operations, gaining foundational industry experience that would support his later roles in quality control and process improvement.
Educational Background and Expertise
Sang Jeon studied Biology at Rutgers, The State University of New Jersey-New Brunswick, earning his Bachelor's Degree from 2007 to 2009. His academic foundation and subsequent professional experiences have equipped him with expertise in biotherapeutics, focusing on re-engineering and improving patient processes. His work often involves analyzing procedural gaps and providing creative solutions to enhance patient care while meeting regulatory requirements.