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David Hattori has extensive work experience in the pharmaceutical industry. David started their career at Actavis (now Allergan) in 2005, where they held various roles including Supervisor of R&D Support, Regulatory Affairs Associate for Specialty Brand Products, Manager of Regulatory Affairs CMC for Specialty Brand Products, and Project Manager for Generics R&D in Semi-Solid Liquids.

In 2016, Hattori joined Teva Pharmaceuticals as a Project Leader for Generics R&D in Semi-Solid Liquids. David then moved to ImmunityBio, Inc. in 2018, where they worked as a Manager and later as a Senior Manager in Regulatory Affairs. David'sresponsibilities at ImmunityBio included providing submission and project management support, facilitating project team meetings, and tracking action items for breakthrough therapy biologics.

Currently, Hattori holds the position of Associate Director of Regulatory Project Management at Vir Biotechnology, Inc. David previously served as the Senior Manager of Regulatory Project Management and as the Senior Manager of Project and Portfolio Management at the same company.

Overall, Hattori has a strong background in regulatory affairs, project management, and R&D in the pharmaceutical industry.

David Hattori, RAC earned a Bachelor of Science degree in Art/Art Studies, General from Northeastern University between 1986 and 1991. David also holds a Regulatory Affairs Certification from the Regulatory Affairs Professionals Society (RAPS). The month and year of obtaining this certification are not provided.