Shruti Dumbre, MSRA, currently serves as Manager of Global Regulatory Affairs for Marketed Products at Takeda since October 2022. Previously, Shruti held the position of Manager in Regulatory Affairs at Karyopharm Therapeutics Inc. from March 2022 to October 2022, and before that, Shruti worked at Takeda in various roles, including Nonclinical Regulatory Submission Writer and Documentation Specialist from September 2018 to February 2022. Early experience includes a role as Documentation Associate at Takeda Oncology and a Quality Assurance Internship at Glenmark Generics Ltd. Shruti earned a Master's degree in Project Management from Harrisburg University of Science and Technology and a Master's degree in Regulatory Affairs in Drugs, Biologics, and Medical Devices from Northeastern University, along with a Bachelor's degree in Pharmacy from the Institute of Chemical Technology.
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Takeda Pharmaceutical
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For more than 230 years, Takeda has brought hope to people around the world through its people-centered and innovation-driven approach to science and medicine. As a global pharmaceutical leader, Takeda focuses on solving unmet needs where it can make a real difference—and on putting patients first. Its therapeutics focus is oncology, gastroenterology, and the central nervous system, as well as vaccines.