07.06.24 | Vollzeit | Steinhausen | Brand Leadership ManagementUnd Koordination in IT-ProjektenErstellung und Pflege von Projektdokumentationen und BenutzerhandbüchernImplementierung und Überwachung von SicherheitsmassnahmenSicherstellung der Einhaltung gesetzlicher und regulatorischer Anforderungen im IT-BereichPflege der Beziehungen zu internen und externen Kunden sowie
Später ansehen01.06.24 | Vollzeit | Baar | Exact SciencesBusiness acumen, intellectual curiosity and creativity, and relevant legal, regulatory and industry issues. - Uphold Company mission and values through accountability, innovation, integrity, quality, and teamwork. - Support and comply with the Company's Quality Management System policies and procedures
Später ansehen22.05.24 | Vollzeit | Steinhausen | Brand Leadership ManagementUnd Koordination in IT-ProjektenErstellung und Pflege von Projektdokumentationen und BenutzerhandbüchernImplementierung und Überwachung von SicherheitsmassnahmenSicherstellung der Einhaltung gesetzlicher und regulatorischer Anforderungen im IT-BereichPflege der Beziehungen zu internen und externen Kunden sowie
Später ansehen03.05.24 | Vollzeit | Frauenfeld | 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 | 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 | 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 | 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 | 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 | 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 | 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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