Quality Engineer II: MedTech PLM & Compliance

KARL STORZ North America is seeking a Quality Engineer II to support product lifecycle management for medical devices. Based in Charlton, MA, you will partner with regulatory affairs, engineering, and quality teams to ensure DHF/DMR, design controls, and GPDP alignment across projects. You will drive audit readiness, risk assessment, and process improvements to maintain compliance and patient safety while delivering quality outcomes in a fast-paced environment.