Hybrid Regulatory Affairs Specialist — FDA Submissions

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

Consider building your career as a Hybrid Regulatory Affairs Specialist I — FDA Submissions at Knowesis Inc.

Are you ready to take on the Hybrid Regulatory Affairs Specialist I — FDA Submissions role at Knowesis Inc.?

We would love to welcome a new Hybrid Regulatory Affairs Specialist I — FDA Submissions to our organisation in Frederick, MD, United States.

For the Hybrid Regulatory Affairs Specialist I — FDA Submissions position at Knowesis Inc., we are reviewing applications now.