• Reviewing Marketing Authorization Application (MAA) dossiers and liaising with the RA department at the company’s headquarters in India.
• Supporting existing and potential clients with regulatory/technical information about company products.
• Preparing and submitting dossiers to health authorities in EU countries using national and decentralized procedures. […]
• Communicating with European customers to develop RA strategies and coordinate submissions. […]
• Ensuring proper maintenance of dossiers, including PSUR submissions, variations, and renewals. […]
• Providing support for the development...