06.05.24 | Vollzeit | Bern | Bavarian Nordic Berna GmbHAssuranceMinimum of 5 years relevant experience in a GxP regulated pharmaceutical/biotechnology industrySolid computer skills including MS Office required - SAP, LIMS, Quality Management Systems skills are a plusAnalytical thinking and problem-solving attitudeMultilingual - at least German and English, written
Später ansehen30.04.24 | Vollzeit | Thörishaus | Bavarian Nordic Berna GmbHAssuranceMinimum of 5 years relevant experience in a GxP regulated pharmaceutical/biotechnology industrySolid computer skills including MS Office required - SAP, LIMS, Quality Management Systems skills are a plusAnalytical thinking and problem-solving attitudeMultilingual - at least German and English, written
Später ansehen03.05.24 | Vollzeit | Zug, Dietikon, Uster, Kriens | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Emmen, Zug, Luzern, Schaffhaus | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Emmen, Zug, Schaffhausen, Dübe | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Emmen, Zug, Luzern, Dübendorf | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Dübendorf, Schaffhausen, Luzer | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Emmen, Zug, Luzern, Dübendorf | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Kriens, Zürich, Dietikon, Uste | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
Später ansehen03.05.24 | Vollzeit | Dietikon, Uster, Zürich, Krien | Daiichi Sankyo Europe GmbHManager, GvP Audits is responsible to support all aspects of pharmacovigilance audits and regulatory inspections including preparation, conduct, tracking and verification of CAPA commitment implementation to assure all are in an acceptable state of compliance. The position will report to the Head
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