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Job Description Summary
Wir suchen einen engagierten Labormitarbeiter zur Untersttzung der Good x Practice (GxP) Aktivitten in unserer Qualittsabteilung. Diese Rolle erfordert die Verwaltung von Qualittssystemen die Einfhrung von Betriebsprozessen und die Sicherstellung der Einhaltung der NovartisQualittsstandards.Job Description
Ihr Verantwortungsbereich:
Behlt die geltenden Standard Operating Procedures (SOPs) GxPkonforme Dokumentationen und Aufzeichnungen innerhalb des Novartis Qualittsmanagementsystems bei.
Durchfhrung und Auswertung von analytischen Ttigkeiten in einem pharmazeutischen Labor
Gewhrleistet die Integritt aller Qualittssicherungsdatenstze und daten soweit anwendbar und die Zusammenarbeit des eigenen Teams mit anderen Funktionen und Abteilungen.
Gewhrleistet ein angemessenes Bildungsniveau GxPKenntnisse.
Untersttzt Qualittsaudits und Inspektionen durch die Gesundheitsbehrde.
Was Sie zur Rolle mitbringen:
Erfahrung in der Qualittssicherung
Analytische Fhigkeiten
alle gngigen Analysentechnologien (e.g. HPLC GC Titration)
Knowhow in der Anwendung von laborspezifischen Software (e.g. Empower Chromeleon TiAmo)
GMPErfahrung
Technologisches Knowhow
Deutsche Sprache
Englische Sprache
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart passionate people like you. Collaborating supporting and inspiring each other. Combining to achieve breakthroughs that
change patients lives. Ready to create a brighter future together and Rewards: Read our handbook to learn about all the ways well help you thrive personally and professionally: to Diversity and Inclusion / EEO:Novartis is committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve.
Accessibility and accommodation:Novartis is committed to working with and providing reasonable accommodation to all individuals. If because of a medical condition or disability you need a reasonable accommodation for any part of the recruitment process or in order to receive more detailed information about the essential functions of a position please send an email to and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities join the Novartis Network here: Some restrictions on flexible working options may apply and will be discussed during interview if applicable.
Skills Desired
Continued Learning Dealing With Ambiguity Gmp Procedures Qa (Quality Assurance) Quality Control (Qc) Testing Quality Standards SelfAwareness Technological Expertise Technological IntelligenceRequired Experience:
IC
Full-Time