Quality Engineer 2

Vor 7 Tagen


Basel, Schweiz Randstad (Schweiz) AG, co Johnson & Johnson Vollzeit
Stellenbeschreibung

"Caring for the world, one person at a time..." inspiriert und vereint die Menschen bei Johnson & Johnson. Wir setzen uns für Forschung und Wissenschaft ein - mit innovativen Ideen, Produkten und Dienstleistungen, um die Gesundheit und das Wohlbefinden der Menschen zu fördern. Die Mitarbeitenden der Johnson & Johnson-Unternehmensfamilie arbeiten mit Partnern im Gesundheitswesen zusammen, um das Leben von mehr als einer Milliarde Menschen jeden Tag auf der ganzen Welt zu verbessern. Wir haben mehr als 260 operative Unternehmen in mehr als 60 Ländern und beschäftigen rund 120'000 Mitarbeitende. Unser weltweiter Hauptsitz befindet sich in New Brunswick, New Jersey, USA.

DePuy Synthes Companies von Johnson & Johnson ist das grösste und umfassendste orthopädische und neurologische Unternehmen der Welt. DePuy Synthes bietet eine unvergleichliche Breite und Tiefe an Technologien, Produkten, Dienstleistungen und Programmen in den Bereichen Gelenkersatz, Trauma, Wirbelsäule, Sportmedizin, Neurologie, Kranio-Maxillofazial, Power Tools und Biomaterialien. Unser breites Spektrum an inspirierenden, innovativen und hochwertigen Angeboten trägt dazu bei, die Gesundheit und das Wohlbefinden von Menschen auf der ganzen Welt zu verbessern.

Am Produktionsstandort für Power Tools und Biomaterialien werden Power Tools in der Endfertigung zusammengebaut und Bioresorbierbare Implantate unter Reinraumbedingungen hergestellt. Als Quality Engineer übernehmen Sie Verantwortung über Quality Engineering Aufgaben im Tagesgeschäft des Quality Operation Teams.

Am Standort Oberdorf profitieren Sie von flexiblen Arbeitszeiten, Home Office, einer lokalen Kantine und diversen Sportangeboten. Sie arbeiten in interdisziplinären Teams und können so stetig voneinander lernen. Es gibt verschiedenste J&J communities die auf Sie warten.

Zu den Haupttätigkeiten gehören:

  • Erstellen und Freigabe von Prüfplänen für den Wareneingang, die Herstellung und die Freigabe eines Produkts
  • Durchführen und Bewerten von Prozessmonitorings
  • Bewerten von Prozessänderungen
  • Systemische Dokumentation qualitätsrelevanter Sachverhalte (Abweichungsmeldungen, CAPA Investigations and Actions)
  • Review und Freigabe von Geräte- und Anlagen-Qualifizierungen sowie Prozessvalidierungen
Functie-eisen

Wen wir suchen:

  • Technische Ausbildung/Studium, Stufe Bachelor oder vergleichbar
  • 2-4 Jahre Erfahrung im Quality Engineering- und MedTech-Bereich
  • Verstehen und Beurteilen von Technischen Zeichnungen und Sachverhalten
  • Erfahrung im Erstellen von Prüfplänen und Abweichungsmeldungen
  • Gute mündliche und schriftliche Deutschkenntnisse, Englisch C1 mündlich und schriftlich
  • Freude und Fähigkeit, in vielfältigen und interdisziplinären Teams Verantwortung zu übernehmen
  • Ein gründliches Verständnis der GMP

Diese Stelle in Oberdorf BL, Schweiz, ist per sofort zu besetzen und vorerst befristet bis 31.12.2024 mit Option auf Verlängerung. Wenn Sie Interesse haben, in einem weltweit führenden Unternehmen im Gesundheitsbereichs Verantwortung zu übernehmen und sich für das Wohl von Patienten einzusetzen, dann senden Sie uns noch heute Ihre Bewerbung auf Deutsch oder Englisch. Oder rufen Sie uns an, wenn Sie Fragen haben

Fabio Romano

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