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 ansehen17.04.24 | Vollzeit | Baar | Ascom Schweiz AGContract Administrator and QA Specialist (m/f/d) Legal DE Frankfurt am Main, RO Cluj-Napoca This job is no longer available. April 22, 2024 Are you ready to revolutionise the healthcare industry through cutting-edge technology? Ascom, a leading global provider of Healthcare ICT and mobile workflow
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