08.05.24 | Vollzeit | Aenova GroupThe production sites and commercial Sales Your profile Relevant degree with demonstrable experience in the pharmaceutical industry, preferably in the finished product operational environment Client-facing experience Strong organisational abilities, dynamic, self-motivated, pro-active approach to taking
Später ansehen03.05.24 | Vollzeit | Frauenfeld, 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 | Frauenfeld, 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 | Frauenfeld, 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 | Frauenfeld, 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 | Frauenfeld, 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 | Frauenfeld, 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 | Frauenfeld, 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 | Frauenfeld, 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 | Frauenfeld, 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
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