Description
The India MDR Regulatory Specialist will advise Halma’s international regulatory teams on India’s Medical Device Regulations, manage regulatory licenses and GEM portal registrations, coordinate with CDSCO and external consultants, and use technology to streamline licensing and process flows. The role requires a degree in Regulatory Management, 1–3 years of relevant experience, core end-to-end India MDR experience, and familiarity with regulatory license platforms; European MDR and FDA exposure is advantageous.
