Teams at Edwards Lifesciences

Support regulatory affairs operations for transcatheter mitral and tricuspid therapies by preparing and managing submission packages, maintaining regulatory records and systems, tracking documentation and schedules, supporting audits/inspections, and driving process improvements, training, and reporting to ensure global regulatory compliance.

Lead digital quality for the ePAC program, driving reengineering and optimization of complex, multi-system business processes. Act as SME for product distribution compliance, translate business needs into functional designs, lead root-cause analysis and testing, provide architecture and platform guidance, mentor administrators, and collaborate with cross-functional stakeholders to ensure regulatory and quality alignment.