Experience 1–3 years (hands-on ownership in Regulatory [CDSCO, ISO, FDA] documentation) About the Role We are seeking an experienced Technical Writer to support our AI team with regulatory and compliance documentation for AI-enabled medical devices and software (SaMD). This role focuses on creating, maintaining, and managing documentation required for FDA submissions and EU MDR compliance , while collaborating closely with AI engineers, quality, regulatory affairs, and clinical teams. You will …