Regulatory Affairs Specialist II — Medical Devices
Sonova Group
A leading global healthcare company is seeking a Specialist II in Regulatory Affairs in California. The role involves preparing regulatory submissions for medical devices, ensuring compliance with FDA and EU regulations, and supporting project teams. Candidates should possess a Bachelor's degree in a scientific discipline, a minimum of 2-3 years of relevant experience, and strong communication skills. Additional perks include comprehensive health benefits and opportunities for career growth in a supportive environment. #J-18808-Ljbffr Sonova Group
Vacancy posted 5 days ago
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