Timothy Reinhardt has worked in the pharmaceutical industry since 1992, including 18 years of quality leadership at Pfizer Inc, with the most recent role as the Director of Manufacturing and Supplier Quality Assessment. This group was responsible for the global quality compliance auditing program for contractors as well internal sites. His previous multifaceted pharmaceutical background is comprised of numerous quality activities in start-up, development and commercial stage organizations with various operations globally. His experience includes the regulations pertaining to gene therapy; sterile liquid, lyophilized and dry powder products; oral liquids; creams; tablets; transdermals; active ingredients and medical devices. In addition to his extensive experience on cross functional teams performing compliance assessments, inspection readiness and due diligences at various sites around the world, Tim was also the former leader of the Pfizer Site Auditor Training certification program as well as a member of the global data integrity assessment team.
Tim obtained his Bachelor’s Degree from the University of California, Davis, his Master’s Degree from San Francisco State University, as well as a professional certificate in pharmaceutical manufacturing from Stevens Institute. Tim will be serving RMC clients as both a Senior Consultant and Site Manager for the RMC North Carolina operations in the Raleigh area.
