David Keese

David Keese

Associate Director Quality Assurance Manufacturing Operations @ Bristol Myers Squibb

About David Keese

David Keese is the Associate Director of Quality Assurance Manufacturing Operations at Bristol Myers Squibb in Devens, Massachusetts, with over 14 years of experience in various roles within the company.

Current Position at Bristol Myers Squibb

David Keese currently holds the position of Associate Director of Quality Assurance Manufacturing Operations at Bristol Myers Squibb, located in Devens, Massachusetts. His role involves overseeing quality assurance processes within the manufacturing operations, ensuring standards are met and maintained across all activities.

Previous Roles at Bristol Myers Squibb

David Keese has a robust history with Bristol Myers Squibb, having served in various roles since 2009. From 2021 to 2023, he was the Senior Manager of Quality Assurance in Massachusetts. Prior to that, he worked as a Quality Assurance Manager in Devens, Massachusetts, for nine months from 2020 to 2021. Additionally, he was the Method Trending Lead from 2016 to 2020 and also held a role as a Quality Assurance Associate from 2009 to 2011.

Experience in Quality Control

David Keese has extensive experience in Quality Control, highlighted by his four-year tenure as Method Trending Lead from 2016 to 2020 at Bristol Myers Squibb. In this role, he focused on maintaining and analyzing quality control data trends, ensuring compliance with industry and regulatory standards.

Career at Medstar Ambulance Inc

Before transitioning to the pharmaceutical industry, David Keese worked as an Emergency Medical Technician at Medstar Ambulance Inc from 2003 to 2009. This role provided him with a foundational understanding of medical and emergency response protocols.

Educational Background

David Keese holds a Bachelor of Science degree in Biology, with a concentration in Molecular Biology, from Fitchburg State College. He completed his studies between 2005 and 2008. His academic background laid the groundwork for his subsequent career in quality assurance and control within the pharmaceutical industry.

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