Sunnyvale, California, United States
FDA-regulated robotic surgical platforms
Spent seven years building and scaling FDA-regulated, safety-critical robotic systems used in live clinical environments, where design errors translate directly to patient risk, recalls, or production shutdowns.
Led mechanical design and production validation for next-generation advanced energy surgical systems, owning end-to-end development from early architecture through design verification, validation, and manufacturing scale-up. This included thermal management of power electronics, durability and safety testing (shock, vibration, thermal, fluid ingress), and close vendor collaboration to ensure DfMA and production robustness.
In parallel, worked on sustaining engineering and supply-chain resilience for advanced energy instruments in active clinical production, including COVID-era supply disruptions. Built internal quality analytics to identify systemic failure modes, prioritize high-risk components, and drive continuous quality and cost improvements across multiple product lines.
This experience shaped my approach to building physical systems: assume failure, validate aggressively, and design for scale and long-term reliability, not just first launch.