03.05.24 | 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 | Uster | 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 | 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 | 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 | 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 | Luzern | 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 | Uster | 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 | 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 | Frauenfeld | 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 ansehen24.04.24 | Vollzeit | Sempach | Randstad Schweiz AGFor our client specialized in Medical Device area, we're looking for a Product engineer administrator Location Lucern canton Position Permanent You will play a crucial role in maintaining and managing SAP basic data in the product engineering domain. You will be responsible for creating
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