22.03.24 | Vollzeit | Kriens, Dietikon, Luzern, Uste | 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 | Kriens, Dietikon, Luzern, Uste | 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, Dietikon, Kriens, Zug | 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, Zürich, Emmen, Scha | 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, Frauenfeld, Zug | 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, Dietikon, Kriens, Zug | 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, Kriens, Dietikon, Scha | 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 Document landscape within pCMC Participating in the preparation and coordination of internal and health authority audits, as well as supporting the timely implementation of inspection findings Collaborating with team members in a role based working environment, as well as building and growing
Später ansehen25.04.24 | Vollzeit | Zürich | Zürich Versicherungs-AktiengesellschaftAnd implementation process - Create Automated Acceptance Testing Scripts as needed. Basic Qualifications - Bachelor degree in Computer Science, MIS. - English Advanced - 5+ years of experience programming in C#.Net and/or VB.Net. - 3+ years of experience with consuming web services and web api - 3+ years
Später ansehen25.04.24 | Teilzeit | Solothurn | Ypsomed AGThe development and implementation of global clinical research projects - Participate to scientific conferences and workshops to maintain industry knowledge and to present scientific data to HCPs - Organization and development of scientific content from scientific symposia - Develop and implement strategies
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