das Hygienekonzept in den Produktionsbereichen und stellen die Erfüllung der relevanten ISO-Normen am Standort sicher Sie planen, initiieren und leiten Untersuchungen zur Ursachenermittlung von Qualitätsabweichungen
in highly regulated environment Ability to plan, manage and execute projects in a product development environment in self-reliant manner Good technical and analytical skills Good interpersonal and
further development is just as great as our additional benefits. Ranging from active health management via flexible working hours and hybrid work all the way to corporate pension plans: everything geared to
responsible to plan technical work packages and deliver them according to quality, delivery and cost targets, in alignment with your project manager. You know and understand production processes and their
similar 3+ years of working experience in product development of medical devices, pharmaceutical packaging or similar Experienced with documentation in highly regulated environment Ability to plan
industrialization projects from idea all the way to transfer to our production sites worldwide. You are responsible to plan technical work packages and deliver them according to quality, delivery and cost targets
plan technical work packages and deliver them according to quality, delivery and cost targets, in alignment with your project manager. You know and understand in details regulatory and technical customer
plan medium-term international or interdisciplinary projects that include several disciplines, e.g. technology development, and further teams, e.g. R&D or site management. In this context, you not only
on the specific topic, compare measurements methods and select the most appropriate You are responsible for the definition of the test methods and the preparation of the test plans You work with
perform and moderate risk analysis (e.g. GMP-RA, FMEA) according to specifications and standards You create, review and update qualification & validation documents (e.g. plan, test plan, protocol, report
des IST-ZustandesGap-AnalyseErarbeitung der Abreichungsstrategie für Endotoxine (3s) Erstellung der erforderlichen Dokumentation bzw. Review und Freigabe der relevanten Q/V Pläne und Berichte Mitarbeit bei der Umsetzung
-relevante Änderungen zu beurteilenReview und Freigabe der relevanten Q/V Pläne und Berichte Unterstützung bei CAPA-Massnahmen sowie Untersuchungen in Zusammenarbeit mit den relevanten Abteilungen Beratende
way to corporate pension plans: everything geared to suit your goals and needs. Discover a special corporate culture where everyone has the opportunity to develop their entire potential. At SCHOTT, you
-relevante Änderungen zu beurteilenReview und Freigabe der relevanten Q/V Pläne und Berichte Unterstützung bei CAPA-Massnahmen sowie Untersuchungen in Zusammenarbeit mit den relevanten Abteilungen Beratende
des IST-ZustandesGap-AnalyseErarbeitung der Abreichungsstrategie für Endotoxine (3s) Erstellung der erforderlichen Dokumentation bzw. Review und Freigabe der relevanten Q/V Pläne und Berichte Mitarbeit bei der Umsetzung
Qualitätssystems Planen, implementieren, durchführen der Produktqualifikation in allen Bereichen in Zusammenarbeit mit den Fachspezialisten Geschäftsprozesse in allen Abteilungen in deren Anwendung überwachen