Technical Program Manager, Regulatory
Jay is currently a Technical Program Manager, Regulatory Affairs at Verily Life Sciences. His role is to support the various project teams as they develop innovative solutions to the challenges faced in healthcare.
Verily is developing tools to collect and organize health data, then creating interventions and platforms that put insights derived from that health data to use for more holistic care management.
His responsibilities at prior positions included pre- and post market regulatory and quality system management of platform based software devices (SaMD and SiMD), artificial intelligence , combination devices, endoscopic devices including investigational and approved products, regulatory project management, original 510(k) filings and supporting various regulatory body audits.
Jay also has experience working with multiple health authorities including the FDA, Health Canada and EU competent authorities.
Jay has a Masters in Medical Device and Diagnostics Engineering from the University of Southern California in Los Angeles where he studied regulatory affairs.
Tuesday, September 24
1:00 PM – 1:55 PM