Jason Rice
About Jason Rice
Jason Rice is a Sr. Specialist in Technical Writing at Bristol Myers Squibb with over 15 years of experience in the pharmaceutical and chemical industries.
Current Position at Bristol Myers Squibb
Jason Rice is currently serving as a Sr. Specialist in Technical Writing at Bristol Myers Squibb in Summit, New Jersey, United States. His role involves creating, reviewing, and managing technical documentation to support various pharmaceutical projects and initiatives.
Previous Work Experience at Celgene
Prior to his current role, Jason Rice worked at Celgene as a Technical Writer, QC Systems and Services from 2019 to 2020 for one year. During his tenure in Summit, NJ, he was responsible for creating and maintaining quality control documentation, ensuring compliance with regulatory standards.
Experience in Quality Control Chemistry at Akorn Pharmaceutical
Jason Rice held the position of Technical Writer, QC Chemistry at Akorn Pharmaceutical from 2016 to 2019 in Somerset, NJ. Over three years, he contributed to quality control chemistry projects, developing and maintaining technical documentation to ensure product quality and regulatory compliance.
Analytical Development Projects at Hovione
Jason Rice spent six years at Hovione in East Windsor, NJ, working as an Analytical Development Chemist from 2008 to 2014. In this role, he was involved in various analytical development projects, focusing on the development and validation of analytical methods for pharmaceutical products.
Educational Background in Chemistry
Jason Rice studied Chemistry with a concentration in Biochemistry at the University of Virginia, earning a Bachelor of Science (B.S.) degree with Distinction from 2001 to 2005. Additionally, he achieved a Regulatory Affairs Certificate: Pharmaceuticals from the Regulatory Affairs Professional Society, from 2016 to 2017, enhancing his expertise in regulatory affairs.