Documentation Manager állás innen: Magyarország

2025. 05. 27. | Teljes munkaidõ | Budapest | SanofiQD plan. Ensure Sanofi architecture of QDs is er simplification and avoid redundancy of Quality Documents Ensure timeliness and quality of Quality documents in the Electronic Document Management System Ensure documents are following the correct workflow stepsPerform a QC step of each

2025. 06. 12. | Teljes munkaidõ | Budapest | SanofiBudapest Hub Transition Lead Hiring Manager Head of Global Transitions Management Location - Budapest 50% Remote working and some travel expected Job type Permanent Full time About the job Our Team This position is part of Business Operations BU, within Global Hub Operations and Transitions

2025. 06. 11. | Teljes munkaidõ | Budapest | SanofiSkills could be critical in helping our teams accelerate progress. Join our global Clinical Sciences and Operation (CSO)’s Clinical Documentation department as a Trial Disclosure Manager (TDM) and you’ll ensure timely public disclosure of protocol information and study results, in line with regulatory

2025. 06. 05. | Teljes munkaidõ | Budapest | SanofiResponsibilities In cooperation with the Global Regulatory Lead (GRL) members of the Global Regulatory Team and Global Project Manager (GPM), develop a comprehensive table of content listing all documents part of CTD. Develop a schedule for individual document draft, review, and approval, predecessor

2025. 06. 02. | Teljes munkaidõ | Budapest | SanofiOf returned, rejected, recalled, or potentially falsified products. Ensuring adherence to national law requirements. Overseeing the management and documentation of the QMS Medical Devices. Managing document management system Proactively participates to achieve Site Quality Risk Assessment, in developing

2025. 05. 30. | Teljes munkaidõ | Budapest | SanofiWriting, trial operations and electronic documentation. We have positions from entry level up to managerial roles, and we can find the best option for you. Global Regulatory Affairs (GRA) ensures that pharmaceutical products comply with regulations and laws in different countries and regions around

2025. 05. 30. | Teljes munkaidõ | Budapest | SanofiSystem. Propose and coordinate remediation plans in case of compliance issues Provide support and direction to the Associate TMF managers, Clinical Documentation Administrators in the processing of TMF documents, and be the main point of contact for TMF Contributors Write the TMF Plan and perform TMF

2025. 05. 30. | Teljes munkaidõ | Budapest | SanofiInventory tracking & reconciliation, final country reconciliation, cost reconciliation and last payments Update databases, manage depot data changes, also file and archive Investigational Product (IP) related documentations Support the inspection documentation collection from IP management perspective