27/03/2024 | Fulltime | Prostějov | E.ON Drive Infrastructure GmbHRelation Management - Control, manage and maintain energy storage and energy management products along the product lifecycle with EDRI's partners and suppliers, incl. - Defining and managing technical product and service requirements - Defining and conducting acceptance tests of new products and features
Save for later22/03/2024 | Parttime, Fulltime | Organon LLCAs presenter. - Share, on a reactive basis, the publicly available areas of interest with SLs and direct them to the appropriate resources for further information. - Provide medical/scientific support, including written documentation and/or verbal interactions for Health Technology Assessments and formulary
Save for later04/03/2024 | Fulltime | NTT DATA Business Solutions AGFunction in accordance with other relevant processes, such as the client's quality management system ■ Be responsible for preparing and drafting the validation documentation Your duties will be ■ Preparing validation plans ■ Performing risk assessments ■ Preparing and reviewing design specifications
Save for later21/03/2024 | Fulltime | Offenbach am Main | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Aschaffenburg | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Kaiserslautern | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Rüsselsheim | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Aschaffenburg | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Mainz | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
Save for later21/03/2024 | Fulltime | Wiesbaden | BioNTech SETo the integrated development plan, clinical development plan, and to regulatory study- or program-related documents such as clinical trial protocols, and -reports, investigator brochures, briefing documents, and market authorization applications Contributes to the execution of the translational and biomarker
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