11.06.24 | Vollzeit | Mainz | BioNTech SEIncluding common programming languages (Python, R, Matlab), software packages, algorithms and affinity with statistics is a plus Preferably experience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality
Später ansehen11.06.24 | Vollzeit | Mainz | BioNTech SETo successfully work in cross-functional complex teams and fast-moving environments Excellent verbal and written communication skills combining business process and technical content You should be able to communicate fluently in German (B2 level) and English Flexible Working Time Mobile Office Work from EU
Später ansehen11.06.24 | Vollzeit | Mainz | BioNTech SETo successfully work in cross-functional complex teams and fast-moving environments Excellent verbal and written communication skills combining business process and technical content You should be able to communicate fluently in German (B2 level) and English Flexible Working Time Mobile Office Work from EU
Später ansehen11.06.24 | Vollzeit | Mainz | BioNTech SEIncluding common programming languages (Python, R, Matlab), software packages, algorithms and affinity with statistics is a plus Preferably experience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality
Später ansehen11.06.24 | Vollzeit | Mainz | BioNTech SEWith a minimum of 7+ years relevant work experience in the IVD industry or biotech/pharma. Robust understanding of IVD medical device regulatory requirements and submission processes for U.S. and E.U. (Rest of World knowledge is a plus) Strategic experience related to the development and implementation of pre
Später ansehen11.06.24 | Vollzeit | Mainz | BioNTech SEWith a minimum of 7+ years relevant work experience in the IVD industry or biotech/pharma. Robust understanding of IVD medical device regulatory requirements and submission processes for U.S. and E.U. (Rest of World knowledge is a plus) Strategic experience related to the development and implementation of pre
Später ansehen11.06.24 | Vollzeit | Mainz | BioNTech SEWith a minimum of 7+ years relevant work experience in the IVD industry or biotech/pharma. Robust understanding of IVD medical device regulatory requirements and submission processes for U.S. and E.U. (Rest of World knowledge is a plus) Strategic experience related to the development and implementation of pre
Später ansehen11.06.24 | Vollzeit | Mainz | BioNTech SEIncluding common programming languages (Python, R, Matlab), software packages, algorithms and affinity with statistics is a plus Preferably experience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality
Später ansehen11.06.24 | Vollzeit | Mainz | BioNTech SEIncluding common programming languages (Python, R, Matlab), software packages, algorithms and affinity with statistics is a plus Preferably experience working in a quality-controlled environment (ISO13485, GCP/GC(L)P) and basic knowledge of assay development processes (IVD devices) Pro-active mentality
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