22.03.24 | Vollzeit | Kriens, Dietikon, Luzern, Uste | 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, Dietikon, Kriens, Zug | 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, Zürich, Emmen, Scha | 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, Frauenfeld, Zug | 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, Dietikon, Kriens, Zug | 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, Kriens, Dietikon, Scha | 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 ansehen25.04.24 | Vollzeit | Aarburg | Franke GesmbHSAP QM/PP Consultant (f/m) 100% - Hybrid - Please wait. Date Apr 23, 2024 Location Aarburg, CH Company franke About Franke We, the Franke company with its three divisions, are a world's leading supplier of products and services for domestic kitchens, the professional foodservice systems
Später ansehen25.04.24 | Vollzeit | Michael Page InternationalMeetings to ensure timely completion of tasks. - Document Management Maintain organized electronic and physical filing systems for confidential documents, contracts, legal
Später ansehen25.04.24 | Vollzeit | Fribourg | Michael Page InternationalThe Successful Applicant - 10+ years experience in Marketing and Sales of the medical device business - 5+ years experience in Product Management - Proficiency with Networks and Laboratory Information Systems (LIS). - Experience in working in a cross-functional, international environment - Solid understanding
Später ansehen25.04.24 | Vollzeit | Michael Page InternationalIs an asset. Affinity with IT, ERP systems (preferably SAP), is crucial. The Successful Applicant Key Accountabilities - Manage a diverse range of projects within the Finance team, spanning from small, short-term initiatives to integral work streams in complex projects. - Collaborate closely with finance
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