Meggan Czapiga is a seasoned professional in global regulatory affairs and diagnostics, currently serving as the Global Regulatory Affairs Devices In Vitro Diagnostics Lead at UCB since January 2021. Prior to this role, Meggan held positions including Senior Director of Companion Diagnostics Programs at Autolus Ltd. and Precision Medicine CDx Leader at GSK. With a strong foundation in research and development from MedImmune, where responsibilities included managing Histopathology, Research Pathology, and Microscopy Labs, and a background as a Staff Scientist at the National Institutes of Health specializing in biological imaging, Meggan brings extensive expertise in translational medicine and diagnostics. Meggan earned a Doctor of Philosophy in Neuroscience from Georgetown University between 1997 and 2000.
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