The Supplier Quality Engineer role supports quality activities for new product introduction and sustaining manufacturing within a regulated medical device environment. Key responsibilities include conducting supplier assessments and audits, reviewing documentation for regulatory compliance with ISO 13485 and 21 CFR Part 820, and managing corrective actions for supplier-related quality issues. The position serves as a vital link between engineering, procurement, and external suppliers to ensure consistent performance and risk mitigation. This opportunity appeals to candidates seeking to work in a collaborative, cross-functional team where they can drive continuous improvement and contribute to critical product launches. The role involves a mix of remote and onsite travel for supplier evaluations.