Document Manager állás innen: Budapest

2025. 05. 24. | Teljes munkaidõ | Budapest | SanofidocumentMonitor workflow steps of each document until approval. Remind authors, reviewers and authorizer as unicate on the approval and effective dates of Quality Documents Ensure the delivery of training of the concerned QDs by creating training link in the Learning Management Systems(s) and preparing

2025. 05. 24. | Teljes munkaidõ | Budapest | SanofiThe world. Opportunities in GRA Chemistry Manufacturing & Control Labeling Submission Management Ilearn Support User Support Data Governance Data Analytics & Reporting Quality Clinical Trial Applications Clinical Sciences & Operations (CSO) transforms the miracles of science into life-changing medicines

2025. 05. 23. | 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. 05. 23. | Teljes munkaidõ | Budapest | SanofiCoordination throughout the project life cycle. Manage transition management documents such as the transition plan, budget, or schedule as needed. Monitor transition progress and create transition status reports for management and stakeholders (e.g., accomplishments, next steps, issues, risks, action items

2025. 05. 23. | 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

2025. 05. 22. | 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. 22. | Teljes munkaidõ | Budapest | SanofiAnd development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Join our global Vaccines Clinical Documenation Record Management team as a Trial Master File (TMF) Manager and you’ll be the part of supporting global activities related

2025. 05. 20. | 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