03.05.24 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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 ansehen01.05.24 | Vollzeit | Zug | JobLeads GmbH | CHF 150’000 - CHF 200’000 Safety, regulatory requirements. - Skilled at simultaneous consideration of scientific data and practical healthcare delivery needs from diverse health systems to optimise medical implementation of innovation. #LI-GSK* Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK
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