25.05.25 | Vollzeit | Neusiedl am See | JobLeads GmbH | € 40.000 - € 60.000 Policies as needed. Collaborate with brokers, insurers, and consultants to ensure policies meet business needs. Deep understanding of policy language and coverage. Manage complex global third-party liability claims, communicate strategies with defense teams and insurers. 2. Cyber Insurance Line Management
Später ansehen23.05.25 | Freelancer, Vollzeit | Burgenland | JobLeads GmbH | € 40.000 - € 60.000 SAS experience is a plus. - Solid understanding of HTA processes, payer requirements, and health economic methodologies. - Excellent attention to detail, scientific writing, and client communication skills. - Ability to work independently and manage time effectively in a remote, fast-paced environment
Später ansehen05.05.25 | Vollzeit | Eisenstadt | JobLeads GmbH | € 40.000 - € 60.000 Management Renew and place global master general and professional liability policies annually. Coordinate with brokers, insurers, and team members to ensure policies meet business needs. Manage complex global third-party liability claims, including communication strategies with defense teams and insurers. 2
Später ansehen24.04.25 | Vollzeit | Burgenland | JobLeads GmbH | € 60.000 - € 80.000 And performance expectations. Negotiation and Contract Management - Lead high-value negotiations to secure optimal terms, pricing, and service levels with suppliers, sponsorship partners, and potential retailers. - Manage and oversee contracts, ensuring that all agreements are fulfilled and compliant with terms
Später ansehen25.03.25 | Vollzeit | Burgenland | JobLeads GmbH | € 60.000 - € 80.000 Your Role at Cabot Cabot Corporation is seeking a GBS Regional Manager, Logistics & Packaging to join the logistics team at one of the EMEA Cabot office locations. The GBS Regional Logistics & Packaging Procurement Manager is responsible to actively manage all Logistics & Packaging procurement
Später ansehen18.01.25 | Vollzeit | Burgenland | JobLeads GmbH | € 40.000 - € 60.000 Role will involve supporting the development and implementation of the Quality Management System with my Medical Device client in order to maintain 2017/745(MDR), ISO 13485, ISO 14971, ISO 9001 and FDA QSR standards and requirements. The QMS includes medical device design and Development, Manufacturing
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