Regulatory Affairs Manager: 510(k) & Global Strategy

Verathon is seeking a Manager, Regulatory Affairs at our Bothell, WA headquarters. This hybrid onsite role leads Regulatory Affairs, overseeing FDA 510(k) submissions and global registrations, and shaping regulatory strategy across Engineering, Clinical Affairs, Quality and Commercial teams.

You will mentor a team of Regulatory Affairs Specialists, manage budgets, and ensure compliance within the QMS, while coordinating with distributors and regulators. Travel up to 10% internationally.