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Deanna Shamsi currently serves as a Senior Regulatory Affairs Specialist at GOJO Industries, with experience in regulatory affairs since May 2010, including a prior role as Analyst II in Drug Regulatory Affairs at Hikma Pharmaceuticals. Responsibilities at Hikma included preparing and submitting Annual Reports, Abbreviated New Drug Applications (ANDAs), New Drug Applications (NDAs), and various amendments to the FDA. Before this position, Deanna held multiple roles at Hikma, such as Specialist II in API Quality and Supplier Management, where the development of technical document templates was emphasized, and Scientist II in Analytical Development and Scientist I in Quality Control, focusing on analytical tasks and testing of API materials. Deanna holds a Bachelor of Science degree in Biology and Chemistry from Ashland University, earned between 2006 and 2010.