Hiring for a Head QARA for a leading medicaldevicecompany
Location : Haryana
Experience -13-18Yrs
Reportees- 7-8ppl
Reports to COO
Profile- To lead and manage global regulatory affairs activities for Active Medical Devices, ensuring compliance with EU MDR 2017/745, CE Marking requirements, ISO 13485, CDSCO, and other international regulatory frameworks. The role will drive regulatory strategy, product registrations, technical documentation, notified body interactions, and lifecycle compliance for existing and recent products
Plz note experience in handling QARA for activemedicaldevices is mandatory