Sr. Regulatory Affairs Specialist

The Senior Regulatory Affairs Specialist leads and executes regulatory strategy for an implantable neurostimulation therapy treating obstructive sleep apnea, supporting global regulatory activities primarily in the United States and European Union. This role involves developing compliant, risk-based regulatory strategies across product development and lifecycle activities while collaborating with cross-functional partners to ensure compliance with global regulatory requirements. The position requires strong regulatory expertise, scientific knowledge, and business acumen to manage submissions and assessments for medical devices.