03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen02.05.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGProduction site in Schaffhausen. Thanks to our innovative products, processes and technologies, Cilag AG is today one of the leading pharmaceutical companies in Switzerland and at the same time a strategic launch and growth site. You will join a diverse team and be responsible for administration of GMP
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