2024. 06. 13. | Teljes munkaidõ | Budapest | Sanovigado Kft.Management [BB1] Farmakovigilancia training-ek tartásaFarmakovigilancia SOP - WI ellenőrzéseAudit/Inspekció részvételCAPA kezelésTörzskönyvezés, Medical Information, Regulatory Intelligence támogatás, Legalább 2 év farmakovigilancia tapasztalat (bármely terület)Magabiztos angol nyelvtudásLife science
Nézze később2024. 06. 13. | Teljes munkaidõ | Budapest | Citibank Europe plc HungaryQuality of local regulatory this position you will use and expand your experience and professional skills for the following responsibilities Create and formulate various reports that detail important aspects of the bank’s financials for the Central Banks and other regulatorsApply and develop
Nézze később2024. 06. 13. | Teljes munkaidõ | Budapest | Deutsche Telekom IT Solutions HUAnd regulatory topicsOptimization of product management instruments/ tools/ methodologiesDocument managementQualificationsVery good written and spoken German (C1-Level) and good English skills (min. B2 - Level)University degree in a business/product management or similar professional educationExperience
Nézze később2024. 06. 13. | Teljes munkaidõ | Budapest | WHC KftHold and issue resolutionMaintains supplier master data as well as initiates new supplier onboarding workflowsIndependently resolves issues within assigned responsibilities by applying given guidelines, policies, and regulatory frameworkSupports sourcing initiatives, including process improvements
Nézze később2024. 06. 13. | Teljes munkaidõ | Budapest | Woltregulatory reporting Proper archiving of the accounting documents Intercompany related tasks Qualifications 2+ years of previous relevant experience Previous knowledge of accounting and IFRS Understanding of accounting processes Good analytical skills Degree in Finance; accounting Prior experience
Nézze később2024. 06. 13. | Teljes munkaidõ | Budapest | SanofiActivities specifically related to the Clinical trials under the European Regulation and its operational processes in the Clinical Trial Information System (CTIS).Activities related to Development Safety Update Report (DSUR) ribute to data quality control (QC), and appropriate data remediation
Nézze később2024. 06. 13. | Teljes munkaidõ | Budapest | IQVIAAnd integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts
Nézze később2024. 06. 12. | Teljes munkaidõ | Budapest | Thermo Fisher ScientificTechnical Service, Regulatory, Legal, Sales, Marketing and Quality orting key AMS Customer Care strategies to drive customer taining database and ensuring quality of yzing and identifying areas for improvement to drive productivity enhancements through strategic
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