16.05.24 | Vollzeit | Mannheim | 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 ansehen16.05.24 | Vollzeit | Mannheim | 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 ansehen16.05.24 | Vollzeit | Mannheim | 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 ansehen16.05.24 | Vollzeit | Mannheim | 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 ansehen16.05.24 | Vollzeit | Mannheim | 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 ansehen16.05.24 | Vollzeit | Mannheim | 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 ansehen16.05.24 | Vollzeit | Mannheim | 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 ansehen16.05.24 | Vollzeit | Mannheim | BASF Services Europe GmbHCompliance. - Strategic Process Documentation You will lead the development and maintenance of robust process documentation for various Global Mobility services. By ensuring clarity, consistency, and efficiency, you will empower our team to deliver exceptional services and achieve operational excellence
Später ansehen16.05.24 | Vollzeit | Mannheim | BASF Services Europe GmbHCompliance. - Strategic Process Documentation You will lead the development and maintenance of robust process documentation for various Global Mobility services. By ensuring clarity, consistency, and efficiency, you will empower our team to deliver exceptional services and achieve operational excellence
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Strategic in Mannheim kostenlos abonnieren.