Senior Regulatory Affairs Lead — Med-Tech Heart Devices
BrioHealth Solutions, Inc.
BrioHealth Solutions is seeking a Senior Regulatory Affairs Specialist to support the BrioVAD LVAS. This role partners with clinical, R&D, quality, and medical affairs teams to drive regulatory planning, submissions, and lifecycle management. You will manage FDA submissions, advise on labeling and study documentation, and help navigate EU MDR and CE marking efforts for class III devices. Candidates should bring strong technical writing and project leadership. #J-18808-Ljbffr BrioHealth Solutions, Inc.
Vacancy posted 2 days ago
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