Principal Regulatory Affairs Specialist - Software Devices
Treace Medical Concepts
- Experience
- 9+ yrs
- Location
- Ponte Vedra, Florida, United States
- Job type
- Full-time
About the role
Bachelor's degree in engineering, science, or technical discipline; 9+ years regulatory affairs in medically regulated environment, 7+ years in medical device (FDA Class II), 2+ years software medical device (SaMD/SiMD); RAC preferred.
About Treace Medical Concepts
Public U.S. medical-device manufacturer serving foot-and-ankle surgeons with bunion and midfoot correction systems.
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