This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Quality Management Systems Specialist based in United States. This role serves as the operational backbone of a regulated Quality Management System within a software-focused medical device environment. You’ll keep an ISO 13485-compliant QMS running day to day while driving CAPA, NCR, document control, audits, and quality activities tied to software releases. The position offers broad cross-functional exposure, working closely with Engineering, Clinical Affairs, Regulatory, and other teams. You’ll help ensure products are released with complete documentation... Read the full ad