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Principal Regulatory Affairs Specialist - Software Devices
None • Ponte Vedra, FL, US • published 2026-10-06 07:33:52.841056
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**Company Description** *At Treace, we are revolutionizing 3D solutions for the treatment of complex bunion deformities. Our innovative, high\-velocity approach enables us to consistently exceed customer expectations, delivering minimally invasive solutions that improve patient outcomes and drive efficiency for healthcare providers. By advancing reproducibility and patient satisfaction, Treace empowers foot and ankle surgeons to achieve better surgical results, reduce healthcare costs, and enhance overall care quality.* *If you're seeking an opportunity to grow in your career while working with a dynamic and diverse team dedicated to meaningful innovation, Treace could be your next great career destination. Together, let's create something greater than ourselves.* **Job Description** **POSITION SUMMARY:** The Principal Regulatory Affairs Specialist will report to the Director of Regulatory Affairs and will work with Product Development, Quality, Operations, and Marketing to support the product development process and meeting all applicable regulatory requirements. The Principal Regulatory Affairs Specialist will work with Marketing, Sales, Legal and Regulatory partners on advertisi...
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