17.05.24 | Vollzeit | Winterthur | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, 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
Später ansehen17.05.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, 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
Später ansehen17.05.24 | Vollzeit | Winterthur | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, 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
Später ansehen17.05.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, 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
Später ansehen17.05.24 | Vollzeit | St. Gallen | CSL ViforHealthcare, aiming to help patients around the world lead better, healthier lives. We are currently looking for a QA Manufacturing Science Manager for our Parenteral Products to join our team in St. Gallen. In this exciting position, you will be in charge of the Quality oversight of GMP data trending
Später ansehen17.05.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, 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
Später ansehen17.05.24 | Vollzeit | Winterthur | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, 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
Später ansehen17.05.24 | Vollzeit | Zürich | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, 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
Später ansehen17.05.24 | Vollzeit | Luzern | Daiichi Sankyo Europe GmbHEnsuring supporting documentation, 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
Später ansehen16.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalInspection Process You will ensure Compliance with Takeda Quality Management System, regulations and standards, manage Compliance Risk Assessments and represnet your department during regulatory inspections. Ensure the oversite of Quality Systems Pocesses. You will lead a permanent Inspection ready status
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