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- Teljes munkaidő
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1-3 év tapasztalat • Német középfok
Főbb feladatok- Regulatory assessment of raw materials, recipes and nutrient profiles
- Creation and updating of regulatory documentation (e.g. list of ingredients, nutrition information, raw material information)
- Review and approval of labels and communication materials in accordance with EU food law
Ma 18:42 -
- Teljes munkaidő
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1-3 év tapasztalat • Nem kell nyelvtudás
Főbb feladatokThe independent analyses of secondary data, including insurance claims, electronic medical record, patient survey, and disease registry....
Ma 17:15 -
- Teljes munkaidő
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1-3 év tapasztalat • Nem kell nyelvtudás
Főbb feladatok- A degree in Public Health, Epidemiology, Outcomes Research, Health Economics or a related scientific field; MSc or PhD in Epidemiology preferred
- Minimum 2 years of hands-on experience with Real World Data, non-interventional study design and analysis
Tegnap 08:16 -
- Teljes munkaidő
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1-3 év tapasztalat • Angol középfok
Főbb feladatokSubject-Matter Expert (SME) for Test Method Development of delivery devices and combination products: Test Method development, including best practices for universal implementation, Test Method Validation/Transfer....
November 17. -
- Teljes munkaidő
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1-3 év tapasztalat • Német középfok
Főbb feladatokas part of DFG sponsored project beginning in January 2026 limited for three years. The Title of the project is: EFFECTS OF LACTOBACILLUS REUTERI DSM 17938 ON THE ACUTE PSYCHOLOGICAL, ENDOCRINE AND IMMUNOLOGICAL STRESS RESPONSE IN HEALTHY CITY DWELLERS. Both preclinical and clinical data support...
November 13. -
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Mobiltelefon • Egészségbiztosítás
- Teljes munkaidő
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1-3 év tapasztalat • Német középfok
Főbb feladatok- Ensuring process adherence for the pre-market procedures
- Completeness of design history files and regulatory submissions
- Regulatory and process conformance for development and maintenance projects as a member of cross-functional teams
November 07. -
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- Teljes munkaidő
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1-3 év tapasztalat • Latin középfok
Főbb feladatok- Lead and support cross-functional projects in regulatory affairs and quality management.
- Identify, interpret, and implement regulatory requirements across global markets, with a strong focus on international registrations outside the U.S. and EU.
Október 29.
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