Documentation állás innen: Magyarország

2026. 04. 27. | Teljes munkaidõ | Budapest | ICONWith physicians, investigators, and study staff to ensure protocol adherence and high-quality data collection. The Clinical Research Nurse will actively participate in the care of study participants, as well as in the preparation and maintenance of clinical trial documentation, supporting the successful conduct

2026. 04. 27. | Teljes munkaidõ | Mór | AdientEnsuring of readiness of suppliers and tooling for relevant components. Managing of launch/launch costs according to budget Ensuring that all quality documentation (PFMEA, Control plan) is prepared and agreed upon internally and by the customer Ensuring the ordering of non-series parts, materials and other

2026. 04. 27. | Teljes munkaidõ | Pécs | Deutsche Telekom IT Solutions HURelated topics. • Good knowledge of process creation and documentation, especially for DevOps. • Certifications for SAFe, ITIL or project management frameworks are a plus. • Knowledge of agile development processes. • High level of customer orientation. • Fluency in written and spoken English. • You

2026. 04. 27. | Teljes munkaidõ | Szeged | Continentaldocumentation, release, enforcement) in a corporate organization - esp. in the area of warehousing, transportation packaging Good knowledge of the ContiTech product portfolio and

2026. 04. 27. | Teljes munkaidõ | Budapest | MatritelArchitecture review sessions - Structuring and maintaining technical documentation - Contributing to cross-domain solutions (data, application, infrastructure) Requirements We are looking for you if you - You have a higher education degree (Bsc, Msc) in IT or a technical field - Have 5+years of experience

2026. 04. 26. | Teljes munkaidõ | Budapest | Silicon LabsMembers with a variety of IT-related tasks and collaborate with other teams to support their needs. Contribute to the continuous improvement of support processes and documentation. Minimum Qualifications An IT degree or equivalent combination of training and/or 1-2 years’ experience in a related field

2026. 04. 26. | Teljes munkaidõ | Budapest | IQVIAReview of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department. May perform medical review of adverse event coding

2026. 04. 26. | Teljes munkaidõ | Budapest | IQVIARegulatory projects under the guidance of senior staff. Ability to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers. Prepares and maintains core clinical trial submission dossiers in accordance with applicable regulatory requirements