In this role, I led the team in test case development and execution, uncovering defects, and formal documentation for the Willow Go and Willow 3.0 breast pump. This included creating automated and manual test cases for integration and system level functional testing, in addition to developing test plans for firmware verification and translating requirements into test cases. I constructed project timelines supporting the FDA 510K filing and communicated test progress and results to stakeholders.

I guided the transition to automated testing, leveraging characterization scripts, with a projected testing time reduction of 50%. My responsibilities included reviewing software requirements, contributing to feature characterization, and documenting uncovered defects in Jira. I collaborated on a cross functional team developing Class II medical devices.