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The Staff Quality Engineer ensures compliance to standards in medical device projects, supporting product development and manufacturing through quality assurance practices, statistical analysis, and risk management.

The Operations Associate III will perform routine tasks in medical device assembly, operate machines, and ensure compliance with safety and production standards.

Lead and manage medical device projects while ensuring adherence to budget, scope, and timelines. Facilitate cross-functional team meetings, communicate project metrics, and negotiate with customers.

The Supervisor I, Process Development oversees production planning, inventory control, and continuous improvement in manufacturing processes while leading a team.

The Senior Staff Process Development Engineer will lead process improvements, validation, and new product introductions for medical devices, focusing on extrusion and balloon development.