Terrie McDaniel has extensive experience in regulatory affairs and quality assurance within the medical device industry. Currently serving as Vice President of Global Quality Assurance, Regulatory Affairs, and Clinical Affairs at Vyaire Medical since May 2021, McDaniel previously held leadership positions at Xenex Disinfection Services and 3M, where responsibilities included leading regulatory and quality assurance teams. A significant tenure at Acelity saw McDaniel progress through various roles, including Interim VP of Global Regulatory Affairs and Sr. Director of QARA Transformation. McDaniel's early career includes management roles at Arrow International and PrisTech Products, along with engineering work at Southwest Research Institute. Academic credentials include an MBA and a Bachelor's in Mechanical Engineering.
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