24.05.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGQuality Support für das MES (Manufacturing Execution Systems) Einführungsprojekt in der sterilen Arzneimittelproduktion - Beurteilung und Freigabe von Q-relevanten Stammdaten, Herstellvorschriften und Prozessanpassungen - Projektarbeit zur Optimierung von Arbeitsabläufen innerhalb der Beurteilung
Später ansehen23.05.24 | Teilzeit | Hemishofen | Lemonfrog GmbHFor a person who can support us on a regular basis. Please refer to the table below to see which days and times suit us. We need someone for about 4 hours per 2 weeks. If you are interested, please send us a message. We will then get in touch with you if you are suitable
Später ansehen21.05.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGDocuments and trainings at the Janssen Schaffhausen site and drive various compliance and business improvements projects. Main Responsibilities - Support issuance, review and approval of GMP Documents (Standard Operating Procedures, Work Instructions etc) in the Documentation Management System TruVault
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
Später ansehen03.05.24 | Vollzeit | Frauenfeld | Daiichi Sankyo Europe GmbHOf Global Audits and Compliance. Plan, schedule, conduct and report Pharmacovigilance audits including Service Providers, systems and processes, license partners and affiliates to assure that all are in an acceptable state of compliance Document audit conduct, findings, CAPA ensuring supporting
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