Salt Lake City, Utah, United StatesLead the development, implementation, and maintenance of software quality processes to ensure compliance with FDA (FDA 21 CFR 820.30), ISO 13485, and other relevant standards(IEC 82304/62304, SaMD/SiMD). Collaborated with cross-functional teams to facilitate the design and development of compliant medical device software. Conducted risk analysis and implemented risk mitigation strategies to e...