Author állás innen: Budapest

2025. 04. 03. | 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. 04. 03. | Teljes munkaidõ | Budapest | ExxonMobil CorporationFamiliarity with hydrocarbon logistics Strong organizational and interpersonal skills; ability to influence others without authority Sense of ownership and commitment to general interest and high standards Ability to work under pressure and work outside of work schedule to resolve operational issues Your

2025. 04. 03. | Teljes munkaidõ | Budapest | MMSTo advance your career. Visit or follow MMS on LinkedIn . This would be a full-time consultancy role, working remotely. Principal Regulatory Strategist Responsibilities Provide consulting and advisory services for complex regulatory issues or projects. Author and maintain documentation

2025. 04. 03. | Teljes munkaidõ | Budapest | Trivium PackagingIs responsible for execution of Technical Maintenance and Security & Authorization of all our SAP systems. Working together with other SAP BASIS consultants and our partner for User Management. Specific responsibilities SAP Basis Activities - Execution of SAP Basis activities on all our SAP systems/instances

2025. 04. 03. | Teljes munkaidõ | Budapest | MOL MagyarországQuality standards in line with industry best practices. - Stakeholder Engagement & Negotiation Drive networking, structuring, and negotiation efforts, strengthening relationships with authorities, partners, and decision-makers to facilitate successful transactions. - Due Diligence & Decision Support

2025. 04. 03. | Teljes munkaidõ | Budapest | KOSTAL Global Business Services CenterAnd local standard reporting - Analyze and prepare main deviations (e.g. versus Budget - Forecast - Actuals) - Prepare PowerPoint presentations, summaries with meaningful messages - insights - Maintain Reporting Library and coordinate reporting cycles - Maintain authorization matrix for reporting

2025. 04. 03. | Teljes munkaidõ | Budapest | AstraZenecaOrganisation. Accountabilities You will manage pharmacovigilance tasks for the AZ product portfolio in the country in alignment with applicable regulations and AstraZeneca Standard Operational Procedures. You will act as the contact person for Pharmacovigilance towards the local health authorities, coordinate

2025. 04. 03. | Teljes munkaidõ | Budapest | SanofiFor the assigned CMO’s. Duties Prepares the technical dossiers for registrations in collaboration with GRA teams and external partners and ensure data entry in regulatory database for Initial registration Site registration Territory extension Variation Renewal Responses to authorities Ensures the compliance