22.03.24 | Vollzeit | Uster | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Dietikon | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Dietikon | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen22.03.24 | Vollzeit | Dübendorf | Daiichi Sankyo Europe GmbHAnd 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 documentation, tracking - verification of CAPA commitment
Später ansehen26.04.24 | Vollzeit | Luzern | jobwinner.chAuf Gruppenebene übernehmen - in einem kleinen, schlagkräftigen Team. GEMÜ ist eine global agierende Industriegruppe im Familienunternehmen mit 27 Ländergesellschaften und über 2'500 Mitarbeitenden. Sie ist führend in der Entwicklung und Herstellung von Komponenten und Systemlösungen, die in zukunftsorientierten
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