22.03.24 | Vollzeit | Dübendorf | 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 | 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 | 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 | 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 | 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 | 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 ansehen11.11.19 | Vollzeit | Dübendorf | BattrionResponsibilities •Execute and optimize manufacturing process for electrode fabrication for lithium ion batteries •Develop new processes together with engineers and scientists •Manage technicians and cleaning staff of production team •Organize production schedules and resources •Ensure that quality is monitored
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