Teresa Feeser
About Teresa Feeser
Teresa Feeser is the Executive Director of Biologics External Manufacturing Quality at Bristol-Myers Squibb in New Jersey, with extensive experience in the pharmaceutical industry.
Current Role at Bristol-Myers Squibb
Teresa Feeser is the Executive Director of Biologics External Manufacturing Quality at Bristol-Myers Squibb. She is based in New Jersey and her role involves managing teams across the world to ensure a robust supply of biologic products to patients. She aligns process and quality systems with Contract Manufacturing Organization (CMO) partners to maintain consistent quality standards.
Previous Experience at Bristol-Myers Squibb
Before taking on her current role, Teresa Feeser has held multiple director-level positions at Bristol-Myers Squibb. These include Executive Director from 2013 to 2014, Director of Business Excellence from 2012 to 2013 in the Biologics Manufacturing & Process Development division, and Director of Quality Operations from 2007 to 2012. In these roles, she was responsible for various aspects of biologics manufacturing and process development.
Experience at Eli Lilly and Merck
Teresa Feeser has extensive industry experience, having worked at Eli Lilly as Manager of MS&T Parenterals from 2004 to 2007 in Indianapolis, Indiana. Prior to that, she spent nine years at Merck in multiple roles related to product release, validation, and operations based in West Point, PA.
Educational Background
Teresa Feeser holds a PhD in Chemical Engineering from Drexel University. This educational background has provided her with a strong foundation in the principles of chemical engineering, which she has applied throughout her career in biologics manufacturing and quality management.