22.03.24 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 ansehen17.04.24 | Vollzeit | Schaffhausen | STORZ ENDOSKOPUnd überführen Systemanforderungen in geeignete Softwarespezifikationen - Sie führen Code- und Dokumentenreviews durch und managen eine normenkonforme Dokumentation des Entwicklungsablaufs - Sie planen den Backlog und tracken die Umsetzung - Ferner stellen Sie die funktionale Sicherheit und Cyber-Security
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