Author állás innen: Budapest

2025. 12. 29. | Teljes munkaidõ | Budapest | Velenosi&MeredithBe legally authorized to work in Portugal. Apply Today Send your CV to ngir@ or connect via LinkedIn /in/sana-jahangir-64a36724b. Take the next step in your career and join a global team shaping the future of social media

2025. 12. 29. | Teljes munkaidõ | Budapest | ParexelRequirements. Advertising & Promotion - guiding compliant communications that balance innovation with patient safety. Chemistry, Manufacturing, and Controls (CMC) - driving product quality and development through technical and regulatory expertise. Regional and Global Health Authority Expertise - leveraging

2025. 12. 29. | Teljes munkaidõ | Budapest | HARMAN InternationalContributor with elevated responsibility, you will provide thought leadership on best practices, define process standards, and serve as the authoritative representative for procurement in enterprise-wide digital and process development initiatives. You will partner closely with cross-functional teams

2025. 12. 29. | Teljes munkaidõ | Budapest | SanofiFuture launches of high-quality and innovative drugs and vaccines. Main responsibilities Focus on initiation of quality documents (QD) workflow management Identify authors, applicable templates sharing, document change request (DCR) communication if applicable, draft generation in QualiPSO (ID

2025. 12. 29. | Teljes munkaidõ | Budapest | Cross Border TalentsGreece, and gain work authorization expediently. - The most important quality a naturally caring and supportive nature that shines through in every customer

2025. 12. 28. | Teljes munkaidõ | Budapest | ComputacenterComplaints ·Coordinating central and general trainings ·Negotiating the dates of annual leaves, holidays ·Approving assets and licenses/authorisations ·Resolves customer escalation in a timely manner to avoid disruption and minimise business impact ·Plans and distributes workload appropriately to ensure

2025. 12. 28. | Teljes munkaidõ | Budapest | SanofiAuthorized Documents, Hierarchy, Relationship Rules, Workflows) Monitor framework adherence and report to senior leadership Establish Qualipso as single source of truth for process documentation Collaborate with Non-GxP Documentation Centre of Expertise Quality Assurance Define and implement documentation

2025. 12. 28. | Teljes munkaidõ | Budapest | HARMAN InternationalCompliance with customs procedures and authorizations, and managing customs valuation, classification, and country of origin determination. You will also handle the preferential Free Trade Agreement FTA) origin solicitation and qualification process, analyze various products and services for classification