Michael Patterson
About Michael Patterson
Michael Patterson is the Strategy and Business Operations Lead at Bristol Myers Squibb, with extensive experience in biopharmaceutical manufacturing and regulatory compliance.
Role at Bristol Myers Squibb
Michael Patterson is currently the Strategy and Business Operations Lead at Bristol Myers Squibb, located in Devens, Massachusetts. Since May 2015, he has been focusing on strategy setting and business process development for the Quality Assurance organization. His role encompasses key responsibilities such as leading strategic initiatives, optimizing business operations, and enhancing quality standards throughout the organization.
Previous Experience at Genzyme
Before joining Bristol Myers Squibb, Michael Patterson worked at Genzyme as the Associate Director of Bulk Manufacturing from 2010 to 2015. During his five-year tenure, he was responsible for overseeing large-scale bulk manufacturing processes, ensuring adherence to GMP standards, and spearheading productivity improvements across various production lines.
Career at Merck
Michael Patterson served as a Senior Facilitator at Merck from 2008 to 2010. In this role, he played a critical part in regulatory inspections and facilitated comprehensive training programs for staff. His expertise in regulatory compliance and GMP documentation development was instrumental in enhancing the overall efficiency and regulatory adherence of the manufacturing processes.
Educational Background
Michael Patterson holds a B.S. in Biological Sciences from the University of Pittsburgh, which he earned between 1997 and 1999. Prior to that, he studied Biology at Penn State University from 1995 to 1996. His academic foundation in biological sciences has provided a solid basis for his extensive career in biopharmaceutical manufacturing and operations management.
Specializations and Expertise
Michael Patterson specializes in downstream technologies, including chromatography, UF/DF, liquid/liquid extractions, and bulk filling. He has a wealth of experience in leading the implementation of comprehensive safety programs and developing training plans for GMP document development and regulatory compliance. His roles have often involved interfacing with domestic and international regulatory agencies to ensure compliance and successful inspections.