Sterilisation Validation Quality Engineer II - Athlone site

A Sterilization Validation Quality Engineer at Medtronic works within the Sterilization Validation department to ensure product sterility and quality across new product development, site transfers, and sustaining activities. The role provides technical leadership on sterilization methodologies, supports regulatory submissions and audits, and helps shape sterility assurance practices globally. It contributes to continuous improvement and cross-functional collaboration to meet GMP and industry standards.