19.04.24 | Vollzeit | Schaffhausen | RandstadSite and drive various compliance and business improvements projects. Your responsibilities Lead improvements projects for documentation and training process Support Implementation of governance structure for documentation and training on the Site Support issuance, review and approval of GMP Documents
Später ansehen11.04.24 | Vollzeit | Schaffhausen | Johnson & JohnsonSite for parenteral products, and we have an impressive pipeline of new and innovative products!Position summaryAs a Senior AQO in the QA Process Parenterals you will join a dynamic team which is responsible for Quality and Compliance guidance, as well as Quality and Aseptic oversight of equipment
Später ansehen11.04.24 | Vollzeit | Schaffhausen | Johnson & JohnsonSite for parenteral products, and we have an impressive pipeline of new and innovative products!Position summaryAs a Senior AQO in the QA Process Parenterals you will join a dynamic team which is responsible for Quality and Compliance guidance, as well as Quality and Aseptic oversight of equipment
Später ansehen29.04.24 | Vollzeit | Schaffhausen | jobwinner.chVon Investitionsprojektideen - Erstellung und Überprüfung von SAP-Projekten sowie Einhaltung der Compliance - Genehmigung von Finanzierungen - Portfoliomanagement von Investitionsprojekten - Kapitalisierung von Investitionsprojekten - Unterstützung individueller Buchhaltungsprojekte auf Anfrage Anforderungen - Nachgewiesene
Später ansehen26.04.24 | 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 ansehen19.04.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGVarious compliance and business improvements projects. Your responsibilities - Lead improvements projects for documentation and training process - Support Implementation of governance structure for documentation and training on the Site - Support issuance, review and approval of GMP Documents (Standard
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