Mark Paciga

Mark Paciga is a Principal Scientist in Regulatory Affairs at Merck, where they have been since 2020. With over 9 years as a Product Quality Reviewer at the FDA, Mark reviewed biotechnology product manufacturing information for various regulatory submissions, including Investigational New Drug Applications and Biologics License Applications. They also served as a Senior CMC Consultant at DataRevive LLC and held a postdoctoral research fellowship at both the Oak Ridge Institute for Science and Education and the National Institutes of Health, focusing on HIV infection and reproductive system development. Mark holds a Bachelor of Science in Zoology/Animal Biology and two PhDs in Physiology from Western University, along with a Master’s degree in Biology from McMaster University.