22.09.24 | Vollzeit | Zuchwil | JobLeads GmbH | CHF 80’000 - CHF 100’000 Training, and educational measures Education Master’s degree with above-average grades in Engineering, Informatics, Economics or in Supply Chain Management/Operations. Knowledge First work experience in Supply Chain Management or Data Analytics projects (internship, working student jobs). Exceptional
Später ansehen06.09.24 | Vollzeit | Zuchwil | JobLeads GmbH | CHF 100’000 - CHF 125’000 And for the identification of cost reduction possibilities. 4. Due to your strong strategic thinking, you are responsible for market analysis throughout request of quotations and supplier decisions including the necessary documentation in accordance with valid guidelines and efficient supplier management. 5. You are part
Später ansehen06.09.24 | Vollzeit | Zuchwil | JobLeads GmbH | CHF 80’000 - CHF 100’000 Strategy relevance to ensure adaptation where needed - You ensure tracking and analysis with the Regions of the category management activities to extrapolate global KPIs Qualifications - Education Completed studies in marketing or business administration or comparable qualification - Experience and know
Später ansehen31.08.24 | Vollzeit | Olten | JobLeads GmbH | CHF 80’000 - CHF 100’000 By agreement) Workload 80-100% Responsibilities - Manage and further develop the Information Security Management System (ISMS) according to TISAX in close collaboration with various business units. - Provide technical leadership for the information security organization at the group level, including local
Später ansehen14.08.24 | Vollzeit | Olten | JobLeads GmbH | CHF 80’000 - CHF 100’000 Qualifications Profile 1. Completed technical or scientific education or equivalent. 2. Several years of experience in working in the field of medical technology products, pharmaceuticals and/or in-vitro diagnostics. 3. Practical experience in the risk management method for medical devices. 4. Practical
Später ansehen11.08.24 | Vollzeit | Olten | JobLeads GmbH | CHF 80’000 - CHF 100’000 Practical experience in the risk management method for medical devices - Practical experience in the application of quality and problem-solving techniques - Knowledge in the interpretation and implementation of regulatory requirements for medical devices (MDR, EN ISO 14971, 21 CFR 820, EN 13485
Später ansehen19.09.24 | Vollzeit | Sort-en-Chalosse | Michael Page InternationalAnd material management tasks according to the daily schedule - Monitor processes against the recipe and MFG documentation, ensuring accuracy and compliance - Actively participate in training activities and manage your individual training plan - Train other associates when required, contributing
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