03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHOr more years First-hand knowledge of GVP Compliance Professional or other related function and familiarity with Oncology, Specialty Medicines and Companion Diagnostic products 7 or more years Experience of direct dealings with Health Authorities, (e.g., FDA, HPFB, MHRA and other European regulatory
Später ansehen31.05.24 | Vollzeit | Emmen | jobwinner.chOpportunities with competitive salaries. The company is based in Schaffhausen directly at the train station and can therefore be reached in just 39 minutes from Zurich. Software Engineer (C+) A software engineer is part of the developer team and implements user stories, game features and engine technologies
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