Author állás innen: Budapest

2025. 06. 28. | Részmunkaidõ | Budapest | SanofiAssociated Administrative & digital regulatory activities Including coordination of administrative and regulatory activities related to administrative changes, Marketing Authorization Transfer (MAT), Orphan Drug Designation (ODD), Pediatric Investigational Plan (PIP) and RPI (Research Product Identification

2025. 06. 27. | Teljes munkaidõ | Budapest | SanofiDemands Serve as the ultimate authority for service management processes Establish governance structures and decision-making frameworks Ensure compliance with service management standards and policies Drive process maturity and continuous improvement initiatives Build and maintain strong relationships

2025. 06. 27. | Teljes munkaidõ | Budapest | SanofiIncluding Marketing Authorization Transfer plan and the transfer of regulatory responsibilities, including MAT plan implementation, local dossier transfers to the partners, and management of regulatory information internally and externally. May represent Global Regulatory Affairs and provide regulatory

2025. 06. 24. | Teljes munkaidõ | Budapest | SanofiRegulations. Context GenAIR PQR The role is responsible for activities related to the automation of PQR authoring through full digitalization. The objective is to support project initiatives to deliver the PQR by leveraging GenAI technology to automate all sections and approval workflows for the sites