July 2022–present
Medical devices
U.S. Food and Drug Administration
Regulatory Scientific Reviewer
- Lead multidisciplinary reviews of medical-device submissions, integrating scientific, clinical, engineering, software, and human-factors evidence.
- Experience across 510(k), PMA, De Novo, IDE, and Pre-Submission pathways, with additional work in postmarket surveillance and human factors.
- Completed a Human Factors Team Lead detail in OHT3, March–July 2026, supporting guidance implementation, reviewer training, and review consistency.