At Eli Lilly, I coordinate Medical Content Approval, regulatory compliance, localization, and submission tracking. I also lead Adobe Experience Manager migration projects and manage Permission Managed Content.
At TAG WORLDWIDE, I managed regulatory submissions and medical device registrations across product lines. I prepared Saudi SFDA applications through the GHAD portal and supported EU MDR and IVDR registrations through EUDAMED.
At Siemens Healthineers and HCL TECHNOLOGIES LTD, I maintained and reviewed IVD and medical device technical documentation, including GSPR and performance reports. I conducted gap assessments and supported documentation remediation and EU CE marking activities.
