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Hybrid Regulatory Affairs Specialist I FDA Submissions

Knowesis

Knowesis is seeking a Regulatory Affairs Subject Matter Expert I to provide specialized regulatory guidance to ensure successful product development and lifecycle management for WPAC initiatives. This expert navigates complex FDA processes for drugs, biologics, and devices to bring acute care capabilities to the military health system. The role requires developing regulatory strategies, preparing submissions (INDs/NDAs/PMAs/510(k)s), and mentoring colleagues on best practices within a hybrid #J-18808-Ljbffr Knowesis

Vacancy posted 2 days ago
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