Description
Intuitive is hiring a Regulatory Affairs Specialist to prepare and submit medical device technical documentation and registration dossiers under India Medical Device Rules, evaluate regulatory impacts of new devices and product changes, coordinate registration strategy, review marketing materials, respond to regulatory inquiries, and support quality management and regulatory projects. The role requires 8–10 years of medical device regulatory affairs experience, a bachelor’s or master’s degree in a relevant life sciences field, and fluency in English; US FDA and ISO 13485 knowledge are preferred. The position is marked as hybrid.
