Innovate in the realm of neurovascular and endovascular products. As a Principal Engineer, lead design projects, mentor R&D teams, and propel product enhancements to meet customer needs and regulatory standards in a fast-paced setting.

Lead the quality assurance team, establishing standards, policies, and management systems to ensure compliance with medical device regulations while driving product development and operational excellence in an innovative robotics environment.

Drive quality excellence in Supplier Quality Engineering, managing supplier collaboration, audits, and employee development. Ensure compliance with FDA and ISO standards while leading continuous improvement initiatives in a dynamic medical device environment.

Take ownership of inventory and cost accounting in a fast-paced medical device manufacturing environment. Enhance accuracy, streamline processes, and partner cross-functionally to facilitate data-driven business decisions.

Shape the future of clinical trials by enabling top-notch support and coordination for successful project execution. This role involves interaction with clinical sites, ensuring compliance, and maintaining data integrity in a fast-paced environment.