Senior Director, Development Quality @ (February 2024 - September 2026)
Director, Development Quality @ (September 2019 - February 2024)
Principal Manager, Quality and Compliance Office gRED Early Development @ (January 2018 - September 2019)
Process Excellence Leader, GCP and GVP @ (April 2016 - December 2017)
Principal Quality Specialist @ (September 2015 - April 2016)
Sr. Quality Specialist (Standards and Process Governance) @ (July 2012 - September 2015)
Regulatory and Compliance Coordinator @ (October 2007 - May 2012)
Clinical Research Coordinator @ Veterans Hospital (July 2006 - July 2007)
Clinical Research Associate @ Synarc (January 2004 - January 2007)
Devon Hyatt Education
Science Leadership Program, Genentech 2018-2018
San Diego State University
MS (Regulatory Affairs)
2009-2011
Lewis & Clark College
BA (Psychology)
2000-2004
Devon Hyatt Skills
GCP
Biotechnology
Medical Devices
Regulatory Affairs
IRB
SOP development
Quality Systems
Regulatory Compliance
Process Quality Improvement
Training Delivery
Clinical Trials
Controlled Documents
Clinical Research
Clinical Development
Quality System
Quality Assurance
Healthcare
Sop
Quality Process Development
Standard Operating Procedure (SOP)
Corrective and Preventive Action (CAPA)
U.S. Title 21 CFR Part 11 Regulation
Pharmaceutical Industry
GxP
Quality Management
Devon Hyatt Summary
Devon Hyatt, based in California, United States, is currently a Executive Director, Clinical Quality Assurance at Jade Biosciences. Devon Hyatt brings experience from previous roles at Denali Therapeutics and Genentech. Devon Hyatt holds a 2018 - 2018 Science Leadership Program, Genentech. With a robust skill set that includes GCP, Biotechnology, Medical Devices, Regulatory Affairs, IRB and more. Devon Hyatt has 2 emails and 1 mobile phone numbers on RocketReach.
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