27.04.24 | Vollzeit, Freelancer | Zürich | KPMG AGWe are looking for a motivated, committed person who is willing to support us on providing high quality advisory services around model lifecycle management, in particular in quantitative model development and validation, working in a dynamic team environment. Your contribution to KPMG - Support
Später ansehen06.04.24 | Vollzeit | Bubikon | JobLeads GmbH | CHF 150’000 - CHF 200’000 In this role you will be responsible for the overall management and coordination of the Swiss sites, including financial, administrative and legal matters. You will also act as the main point of contact for the Westermo Group and other external stakeholders. Duties and Responsibilities - Manage and oversee
Später ansehen22.03.24 | Vollzeit | Uster | 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 | 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 | 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 | 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 | 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 | 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 | 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 | 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
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