Joshua Davis

Joshua Davis has worked for a variety of companies since 2012. Joshua began their career as a Research Intern at the Massachusetts General Hospital - Molecular Pathology Unit. Joshua then moved on to a Research Assistant position at the Harvard NeuroDiscovery Center/ Brigham and Women's Hospital in 2013, followed by a Biology Tutor position at Northeastern University. In 2015, they became a Gene Editing Specialist at Transposagen Biopharmaceuticals. In 2016, they worked as a Research Associate at the Broad Institute of MIT and Harvard. In 2017, they held several roles at Regulatory and Quality Solutions LLC (R&Q), including Consulting Manager, Senior Regulatory Specialist, Associate Consulting Manager, Senior Regulatory Specialist, Senior Regulatory Affairs Specialist, and Regulatory Affairs Specialist. Joshua also held a Regulatory Affairs position at AxioMed, LLC in 2017. Finally, they have been a Regulatory Affairs Manager at Vyaire Medical since 2020, and is currently a Regulatory Affairs Manager at Neocis.

Joshua Davis attended Northeastern University from 2010 to 2015, where they earned a Bachelor of Science (BS) in Biology. Joshua then went on to complete a Regulatory Affairs Training Program at Duke University in 2016. After that, they returned to Northeastern University and obtained a Master of Science (M.S.) in International Regulatory Affairs for Drugs, Biologics, and Medical Devices in 2018.