Gary Miller has over 20 years in the R&D and manufacturing areas in the pharmaceutical industry. His hands-on experience includes investigations (product and manufacturing), product development, manufacturing, quality, auditing, regulatory, project management, and laboratory management. Throughout Gary's career, he has worked for some of the largest pharmaceutical companies in the world. These include Mylan, Par, Actavis / Teva, and Purdue Pharma.
Since consulting, Gary has been performing FDA Mock Audits (both domestically and internationally), developing SOP procedures for start-up manufacturing site, and performing gap analysis of batch records for a Compounding Facility (503b).
Gary has published paper in the Journal of Chromatography and presented a poster at the Eastern Analytical Symposium in New Jersey. He was also awarded the Boys Scouts of America Eagle Scout Award.