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Donald Ellis has over 25 years of experience in the medical device industry. Donald began their career in 1993 at Sherwood - Davis & Geck as the Director of International Regulatory Affairs. Donald then moved to Eastman Kodak Company in 1998 as the Senior Director of Global Regulatory and Clinical Affairs & Quality Systems. In 2005, they joined Medtronic as the Vice President of Regulatory Affairs & Quality Systems and Senior Director of Corporate Quality. Donald then moved to Ventana Medical Systems in 2007 as the Vice President of Regulatory Affairs & Quality Systems. In 2008, they joined Illumina as the Senior Director of Quality and was responsible for establishing policies and procedures at domestic and international facilities that were consistent with global quality system requirements. From 2011-2016, they held various positions at STAAR Surgical and Aragen Biosciences. In 2016, they joined NuFACE as the Head of R&D Projects, Quality & Regulatory Affairs and Head of Quality & Regulatory Affairs. Donald is responsible for establishing cross functional project specific teams from design to distribution, obtaining clinically relevant research to support commercialization strategy and positioning, and managing the Regulatory Affairs, Quality Assurance, Clinical Affairs and aspects of the product development activities for NuFACE.

Donald Ellis attended Hampton University.