Global Regulatory Affairs Manager - 510(k) & Strategy

Verathon seeks a Manager, Regulatory Affairs to lead the Regulatory Affairs and Quality Assurance Team from its Bothell, WA headquarters. This hybrid onsite role focuses on FDA 510(k) submissions, global registrations, and regulatory strategy across the device portfolio.

You will mentor Regulatory Affairs Specialists, manage budgets, and collaborate with Engineering, Clinical, and Commercial teams to ensure timely market authorizations and compliance. Up to 10% travel required.