2026. 01. 30. | Teljes munkaidõ | Budapest | Tech PeopleAnd accurate payroll information Deliver payroll‑related training during induction and internal development programs Participate in meetings, projects, and continuous learning activities to stay updated on payroll regulations Act as backup for payroll colleagues as part of the team’s backup plan Requirements
Nézze később2026. 01. 30. | Teljes munkaidõ | Budapest | AbbVieProvide expert scientific advice for assigned products and related TAs, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e. pricing and reimbursement dossiers
Nézze később2026. 01. 29. | Teljes munkaidõ | Budapest | ParexelBe office or home based in various European locations. As the Regulatory Affairs Consultant you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products. Primary Tasks
Nézze később2026. 01. 29. | Teljes munkaidõ | Budapest | IQVIAOur ever-growing Lifecycle Safety Medical team is expanding. We are hiring Associate Medical Safety Directors in Portugal, Hungary, Slovakia, Romania, Bulgaria, Serbia, Ukraine and Croatia. The role participates in all aspects of the Medical Safety activities as per scope of work. This includes
Nézze később2026. 01. 29. | Teljes munkaidõ | Budapest | Celanese CorporationOverview Position Summary As a Customer Service Specialist, Order Management, you will serve as a key expert within our EMEA Customer Service organization. You will manage complex order‑to‑cash activities, represent the Customer Service function in cross‑functional initiatives, and act
Nézze később2026. 01. 29. | Teljes munkaidõ | Budapest | Randstad HungaryMigration activities, preparation, and requirement gathering. - Optimize and refactor code where necessary to ensure system performance. - Coordinate with vendors and contribute to front-end (GUI) configuration. - Collaborate effectively across remote teams and manage diverse stakeholder groups
Nézze később2026. 01. 29. | Teljes munkaidõ | ParexelBe office or home based in various European locations. As the Regulatory Affairs Consultant you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products. Primary Tasks
Nézze később2026. 01. 28. | Teljes munkaidõ | Budapest | Syngenta GroupWith data protection laws and regulations. In addition, you will support our third-party risk management program. Whilst working directly with HR teams across the business, you will identify potential privacy risks and supporting mitigation activities as per data protection legal requirements. Reporting
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