Kassi Knight
Regulatory Affairs Specialist | M.S. in Regulatory Science | Medtronic | Class II and III Devices | FDA | EU MDR
- Role
- Regulatory Affairs Specialist at Medtronic
- Location
- Naples, FL, US
- LinkedIn followers
- 500 followers
About Kassi Knight
Regulatory Affairs Specialist with over 6 years of experience in the medical device industry, currently supporting Class II change control at Medtronic. I bring hands-on expertise in regulatory operations, EU MDR compliance, and technical documentation, including (e)IFUs and labeling.I completed my Master’s in Regulatory Affairs (August 2025), equipping me with advanced training in global submissions, FDA requirements, and strategic regulatory planning.Known for my attention to detail and process-oriented mindset, I thrive in fast-paced environments where compliance, collaboration, and innovation intersect. I’m passionate about improving systems, documenting complex workflows clearly, and ensuring patient safety through high-quality regulatory work.My goal: to grow into leadership roles where I can help shape regulatory strategy, streamline processes, and bring safe, effective medical products to global markets.
Experience
Regulatory Affairs Specialist
Dec 2024 — Present · Naples, FL, US
Cardiac Surgery
Education
University of Minnesota
Bachelor of Science - BS, Environmental Science, Policy and Management
Arizona State University
Master's Degree, Regulatory Science
University of Minnesota
Bachelor of Science, Environmental Science
Arizona State University
Master of Science - MS, Regulatory Science
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