22.03.24 | Vollzeit | Zug | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zug | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zug | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zug | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zug | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen22.03.24 | Vollzeit | Zug | Daiichi Sankyo Europe GmbHImplementation are conducted within the electronic quality management systems in a timely manner Support all aspects of pharmacovigilance regulatory inspections including preparation, conduct, coordinating responses, evaluating supporting documentation, tracking and verification of CAPA commitment implementation
Später ansehen24.04.24 | Vollzeit | Zug | www.stellenmarkt.deMICROSAR OS ? Experience in working with version management tools, ideally MKS - PTC Integrity - Understanding of software engineering methods and experience in development tools - Knowledge of the relevant standards (e.g. AutoSpice, ISO 26262) will be an advantage Wir bieten - A highly motivated team
Später ansehen24.04.24 | Freelancer, Vollzeit | Zug | www.stellenmarkt.deTo the hosting infrastructure, the application design and the DB design. Data sources include PI, SAP, Synergie Life and AIM. Access to the systems will be the responsibility of the Project manager. These data sources are part of client's landscape and are already documented - Used tools Atlassian Confluence
Später ansehen23.04.24 | Vollzeit | Zug | Klett und Balmer AGBetrieb sicher und übernimmst den 2nd-Level-Support. Deine Qualifikation - Du verfügst über einen Abschluss mit IT-Background. - Du hast Erfahrungen als Projektleiterin/Projektleiter und im Requirements Engineering. - Deine Problemlösungskompetenzen sind ausgeprägt. - Du denkst mit, bringst
Später ansehen23.04.24 | Vollzeit | Zug | Klett und Balmer AGBetrieb sicher und übernimmst den 2nd-Level-Support. Deine Qualifikation – Du verfügst über einen Abschluss mit IT-Background. – Du hast Erfahrungen als Projektleiterin/Projektleiter und im Requirements Engineering. – Deine Problemlösungskompetenzen sind ausgeprägt. – Du denkst mit, bringst
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