16.04.24 | Vollzeit | Zürich | JobLeads GmbH | CHF 150’000 - CHF 200’000 Of mentorship to the team - Improved efficiency Set the team’s priorities appropriately. Ensure that work outputs are timely and of the highest quality - Manage the S/4 Hana Conversion for FI, CO, TR and BOFC - Global communication Verbal and written communicate with global customers to gather information
Später ansehen13.03.24 | Vollzeit | Hinwil | BELIMO Automation AGDevelopment, architecture, product management) and external test centers- Active participation on the review of requirements for new features- Define and establish Verification Processes- Ensure appropriate reporting of the verification activities (test plans, test cases, test scripts, test results
Später ansehen22.03.24 | 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
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