Responsible for making applications, clarifying to queries,
following up with CDSCO for import license of IVD devices and medical devices regulated under Medical Device Rules 2017.
Following up with CS team to get the Field Safety Corrective Actions implemented for HDX products.
Getting the Product Change Notifications implemented for HDX products.
Performing Quality system audits of suppliers and buss. partners. Supporting zone countries like Bangladesh, Sri Lanka, Nepal & Maldives for regulatory requirements related to IVD products.
Job ID: 104004
Organization: Siemens Healthineers
Experience Level: Experienced Professional
Job Type: Full-time