11.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SEExperience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality and a genuine interest and understanding of the area of expertise and the science supporting BioNTech´s development programs Ability to manage
Später ansehen11.06.24 | Vollzeit | Ludwigshafen am Rhein | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen11.06.24 | Vollzeit | Frankfurt am Main | BioNTech SEExperience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality and a genuine interest and understanding of the area of expertise and the science supporting BioNTech´s development programs Ability to manage
Später ansehen11.06.24 | Vollzeit | Kaiserslautern | BioNTech SEExperience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality and a genuine interest and understanding of the area of expertise and the science supporting BioNTech´s development programs Ability to manage
Später ansehen11.06.24 | Vollzeit | Kaiserslautern | BioNTech SEExperience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality and a genuine interest and understanding of the area of expertise and the science supporting BioNTech´s development programs Ability to manage
Später ansehen11.06.24 | Vollzeit | Kaiserslautern | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen11.06.24 | Vollzeit | Aschaffenburg | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen11.06.24 | Vollzeit | Offenbach am Main | BioNTech SERegulatory specialists, and program managers as well as diagnostic partners. You will play a vital role in the planning, execution, and management of clinical trials for medical devices and IVDs. Independently coordinate IVD and/or companion diagnostics (CDx) Co-development projects as SME. Contribute
Später ansehen11.06.24 | Vollzeit | Kaiserslautern | BioNTech SEExperience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality and a genuine interest and understanding of the area of expertise and the science supporting BioNTech´s development programs Ability to manage
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