Global Regulatory Affairs Lead — Medical Devices

Katalyst CRO is seeking a Regulatory Affairs Lead to steer global regulatory strategies, submissions, and lifecycle management for advanced ultrasound devices. You will manage a team of regulatory professionals and coordinate with Clinical and Global Regulatory Affairs to ensure timely approvals in key markets including FDA, EU MDR, and NMPA.

The role demands strong communication, strategic thinking, and the ability to navigate evolving regulatory landscapes across multiple jurisdictions while

Consider building your career as a Global Regulatory Affairs Lead — Medical Devices at Katalyst CRO.

We are looking to fill the Global Regulatory Affairs Lead — Medical Devices position at Katalyst CRO in Atlanta, GA, United States.

The Global Regulatory Affairs Lead — Medical Devices role at Katalyst CRO is now open for applications in Atlanta, GA, United States.