11.06.24 | Vollzeit | Wiesbaden | BioNTech SEMilestones, risks, and opportunities Critically review development documentation e.g., presentations on analytical performance data, summary of verification plans and reports, clinical performance study plans/reports, performance evaluation reports. Confirming milestone achievement as well as approval
Später ansehen11.06.24 | Vollzeit | Hanau | BioNTech SEInvolving internal- and external Supply Chain partners as well as the required master data structure or clinicial study data. Your focus is mainly but not only on individualized pharmaceutical products and clinical trials. You will manage and develope the corresponding team. Design of requirements
Später ansehen11.06.24 | Vollzeit | Darmstadt | BioNTech SEInvolving internal- and external Supply Chain partners as well as the required master data structure or clinicial study data. Your focus is mainly but not only on individualized pharmaceutical products and clinical trials. You will manage and develope the corresponding team. Design of requirements
Später ansehen11.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEMilestones, risks, and opportunities Critically review development documentation e.g., presentations on analytical performance data, summary of verification plans and reports, clinical performance study plans/reports, performance evaluation reports. Confirming milestone achievement as well as approval
Später ansehen11.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEInvolving internal- and external Supply Chain partners as well as the required master data structure or clinicial study data. Your focus is mainly but not only on individualized pharmaceutical products and clinical trials. You will manage and develope the corresponding team. Design of requirements
Später ansehen11.06.24 | Vollzeit | Aschaffenburg | BioNTech SEInvolving internal- and external Supply Chain partners as well as the required master data structure or clinicial study data. Your focus is mainly but not only on individualized pharmaceutical products and clinical trials. You will manage and develope the corresponding team. Design of requirements
Später ansehen11.06.24 | Vollzeit | Hanau | BioNTech SEInvolving internal- and external Supply Chain partners as well as the required master data structure or clinicial study data. Your focus is mainly but not only on individualized pharmaceutical products and clinical trials. You will manage and develope the corresponding team. Design of requirements
Später ansehen11.06.24 | Vollzeit | Kaiserslautern | BioNTech SEMilestones, risks, and opportunities Critically review development documentation e.g., presentations on analytical performance data, summary of verification plans and reports, clinical performance study plans/reports, performance evaluation reports. Confirming milestone achievement as well as approval
Später ansehen11.06.24 | Vollzeit | Aschaffenburg | BioNTech SEMilestones, risks, and opportunities Critically review development documentation e.g., presentations on analytical performance data, summary of verification plans and reports, clinical performance study plans/reports, performance evaluation reports. Confirming milestone achievement as well as approval
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