2025. 12. 11. | Teljes munkaidõ | Budapest | ParexelWith health authority requirements. The role can be home or office based in various European locations. Role Responsibilities Support global and/or local regulatory teams with comprehensive understanding of regional and global regulatory requirements Manage post-authorization lifecycle maintenance procedures
Nézze később2025. 12. 11. | Teljes munkaidõ | Budapest | ParexelManagement across multiple regions. The role can be home or office based in various European locations. Role Responsibilities Support Global Labelling, Regulatory (Clinical/Safety), or Medical Writing teams for labelling updates Manage Company Core Datasheet (CCDS) implementation into labelling and artworks
Nézze később2025. 12. 10. | Teljes munkaidõ | Budapest | ParexelBe office or home based in various European locations. As the Regulatory Affairs Consultant you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products. Primary Tasks
Nézze később2025. 12. 03. | Teljes munkaidõ | Budapest | ParexelThe product lifecycle while serving as the primary liaison between Regulatory Affairs and various stakeholders. The role can be home or office based in various European locations. Role Responsibilities Prepare Label updates for EU, US and ROW markets Coordinate readability testing Coordinate and manage
Nézze később2025. 11. 13. | Teljes munkaidõ | Budapest | ParexelDelivering both strategic and operational regulatory input to cross-functional teams. The role can be home or office based in various European locations. Key Responsibilities EU Product Information Management Create, update and maintain EU Product Information in line with CCDS, Agency RTQ, and current
Nézze később2025. 11. 26. | Teljes munkaidõ | Budapest | ParexelIn regulatory affairs while working with a diverse range of clients and stakeholders. The role can be office or home based. Role Responsibilities - Manage lifecycle maintenance activities, including renewals, variations, and responses to deficiency letters - Coordinate submission and management work in Veeva
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