Teams at Merit Medical Systems, Inc.

Lead process engineering efforts on night shift to improve equipment reliability, OEE, yield and quality. Manage automation/upgrades, validation, maintenance prioritization, capital spending, cross-functional continuous improvement, and regulatory compliance in a cGMP medical device manufacturing environment.

Participate in product engineering to validate and verify medical device designs, manage sustaining engineering project costs and schedules, coordinate cross-functional development, support cost reduction and technical line support, and ensure compliance with safety and quality systems.