Job descriptionRegulatory Officer for Medical Devices - DMF submission for US, Health Canada, EU, India, China and other countries as per requirements - Indian MDR (CDSCO) license applications - Maintain regulatory documentation for all input materials received from suppliers - USP testing & Biocompatibility testing of products to maintain - Post Market Surveillance of products - Customer query to resolve for regulatory topics - Regulatory agency query to resolve - Audit compliance Powered by JazzHR