03.05.24 | Vollzeit | Kriens | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Emmen | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Dübendorf | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Schaffhausen | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Zug | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen03.05.24 | Vollzeit | Dietikon | Daiichi Sankyo Europe GmbHDocumentation, tracking - verification of CAPA commitment implementation 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
Später ansehen25.04.24 | Vollzeit | Zug | JobLeads GmbH | CHF 150’000 - CHF 200’000 @ Office Timing Mon - Fri 900 - 1700 #J-18808-Ljbffr
Später ansehen11.05.24 | Vollzeit | Zug | NonStop Consulting | And support a group of countries in accounting and reporting activities, ensuring compliance with IFRS standards and timely financial reporting during monthly, quarterly, and annual closings. - Establish strong relationships with Corporate Functions, providing technical guidance and support
Später ansehen03.04.24 | Vollzeit | Rotkreuz | Lucerne University of Applied Sciences and ArtsEnvironment with the opportunity to further develop your own ideas and position yourself in your field of research- Participation in high-profile conferences and workshops (based on publication acceptances)- Flexible working time and placeHow to applyIf we got your interest, please apply by submitting
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