Description
The role leads and motivates a cross-functional hybrid agile team delivering compliance, supply continuity, and quality projects for a blood specimen collection product group. Responsibilities include backlog decomposition, sprint planning, agile project management, phase-gate process compliance, and completion of Design History File and Change Control documentation. The position requires a relevant engineering degree, at least 10 years of experience, 5 years of project management experience, and experience in medical device and regulated environments; medical device product development, FDA or other regulated-environment experience, and a six-sigma background are preferred.
