The Design Quality Engineer role supports Enovis's medical technology division by ensuring product safety, quality, and regulatory compliance throughout the design and manufacturing lifecycle. Key responsibilities include leading risk analysis through DFMEAs, authoring quality procedures and work instructions, and serving as a subject matter expert during ISO and FDA audits. The position also involves reviewing design documentation, managing nonconforming materials, and driving corrective actions for device failures. This opportunity appeals to candidates seeking to contribute to a mission-driven culture focused on improving patient outcomes through continuous innovation. The role offers a collaborative environment within a global organization, requiring minimal travel and providing a clean, professional office setting.