17.05.24 | Vollzeit | Zürich | Solveva AGThe better idea wins- You can empathize with clients, listen, ask the right questions for clarifications, manage expectations- You can deal with sometimes vague requirements and see them as creative challenges- You give engaging presentations, produce clear reports, and always keep an eye on documentation
Später ansehen03.05.24 | Vollzeit | Zürich | 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 | Zürich | 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 | Zürich | 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 | Zürich | 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 | Zürich | 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 | Zürich | 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 | Zürich | 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 | Zürich | 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 | Zürich | 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
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