20.06.24 | Vollzeit | Kronberg im Taunus | Procter & Gambleelectronic devices and the electronic/mechanical technology behind them? You are a problem solver, and you embrace new technology in your private and professional life? Our open roles are as diverse as our employees. You could be starting in Product Design, Mechanical Design, Electronics, Embedded Software
Später ansehen16.06.24 | Vollzeit | Darmstadt | JobLeads GmbH | 100.000 € - 125.000 € Your role We love consulting! Do you? As the company's internal consultancy, we drive projects across all our business sectors, ranging from Healthcare to Life Science, Electronics, and Group Functions. Our approx. 75 highly qualified colleagues from external consultancies, major industry players
Später ansehen06.06.24 | Vollzeit | Mainz | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Darmstadt | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Aschaffenburg | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Mannheim | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Frankfurt am Main | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Darmstadt | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
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