22.03.24 | Vollzeit | Uster, Frauenfeld, Zug, Dietik | 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 | Schaffhausen, Dübendorf, Krien | 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 | Dietikon, Uster, Luzern, Züric | 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 | Emmen, Zürich, Luzern, Dietiko | 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 | Schaffhausen, Dübendorf, Krien | 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 | Luzern, Emmen, Zürich, Dietiko | 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 | Dietikon, Uster, Luzern, Züric | 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 | Frauenfeld, Zug, Kriens, Düben | 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 | Dübendorf, Schaffhausen, Krien | 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 ansehen17.04.24 | Vollzeit | Basel (Basel-Stadt) | ACHIEVA Group Limited | CHF 72 / Stunde Assessments Being an expert and first level support for relevant quality systems (e.g. Cornerstone, Veeva OneQMS, QualityDocs, QRM,) Managing changes and deviations, as well as corrective and preventive actions in consultation with QA Provide expert support to monitor, update, and adapt the GMPrelevant
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