20.09.24 | Vollzeit | Sarnen | Universal-Job AGWas ist meine Funktion? - Leiten und Unterstützen von Kunden-, Optimierungs- und Verbesserungsprojekten im entsprechenden Bereich - Verantwortung für die Einführung neuer Produkte in die Waferproduktion - Erstellen von Projektplänen und Ressourcenanforderungen - Überwachen und Steuern des Projektbud
Später ansehen20.09.24 | Vollzeit | Stalden (VS) | LonzaAreas (e.g. seed train, main cultivation or harvest) for the production of therapeutic proteins with either mammalian or microbial expressions systems (Bioprocess Engineer USP) In charge of one or more defined DSP areas (e.g. capture, polishing or filling) for the purification of therapeutic proteins
Später ansehen20.09.24 | Vollzeit | Stalden (VS) | LonzaSciences in order to support our growth in several business units. Key responsibilities Assignment in various functions within the production facilities in compliance with safety regulations and consideration of cGMP quality requirements. Recognition, interpretation and elimination of deviations Execution
Später ansehen20.09.24 | Vollzeit | Stalden (VS) | LonzaSciences in order to support our growth in several business units. Key responsibilities Assignment in various functions within the production facilities in compliance with safety regulations and consideration of cGMP quality requirements. Recognition, interpretation and elimination of deviations Execution
Später ansehen20.09.24 | Vollzeit | Stalden (VS) | LonzaSciences in order to support our growth in several business units. Key responsibilities Assignment in various functions within the production facilities in compliance with safety regulations and consideration of cGMP quality requirements. Recognition, interpretation and elimination of deviations Execution
Später ansehen20.09.24 | Vollzeit | Stalden (VS) | LonzaFacilities are high automated with DeltaV and MES systems. In a GMP environment the assets have to be kept compliant and fulfill readiness for pharmaceutical production. The batches for our customers are continuously running wherefore a stable electrical MSR environment is crucial. Key responsibilities
Später ansehen20.09.24 | Vollzeit | Stalden (VS) | LonzaAnd the implementation and control of defined measures Assist document preparation (e.g. electronic batch records, SOPs) specific to the assigned production area Review production documentation and work on deviations, change requests and implementation of CAPAs to ensure high-quality GMP standards Engage in Capital
Später ansehen20.09.24 | Vollzeit | Stalden (VS) | LonzaFacilities are high automated with DeltaV and MES systems. In a GMP environment the assets have to be kept compliant and fulfill readiness for pharmaceutical production. The batches for our customers are continuously running wherefore a stable electrical MSR environment is crucial. Key responsibilities
Später ansehen20.09.24 | Vollzeit | Stalden (VS) | LonzaFacilities are high automated with DeltaV and MES systems. In a GMP environment the assets have to be kept compliant and fulfill readiness for pharmaceutical production. The batches for our customers are continuously running wherefore a stable electrical MSR environment is crucial. Key responsibilities
Später ansehen18.09.24 | Vollzeit | Stalden (VS) | LonzaFacilities are high automated with DeltaV and MES systems. In a GMP environment the assets have to be kept compliant and fulfill readiness for pharmaceutical production. The batches for our customers are continuously running wherefore a stable electrical MSR environment is crucial. Key responsibilities
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