Lead Specialist Maintenance Technician

vor 2 Wochen


Schaffhausen, Schaffhausen, Schweiz Johnson & Johnson Vollzeit

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function: Supply Chain Manufacturing

Job Sub Function: Manufacturing Process Improvement

Job Category: Business Enablement/Support

All Job Posting Locations: CH008 Cilag AG, Schaffhausen

Job Description:

Über Innovative Medizin

Unsere Expertise in innovativer Medizin wird von Patienten beeinflusst und inspiriert, deren Erkenntnisse unsere wissenschaftlich fundierten Fortschritte fördern. Visionäre wie Sie arbeiten an Teams, die Leben retten, indem sie Medikamente von morgen entwickeln.

Begleiten Sie uns auf unserem Weg, während wir Therapien weiterentwickeln, Heilmitteln finden und den Übergang von der Forschung ins echte Leben ermöglichen, immer im engen Austausch mit unseren Patienten, um sie bei jedem Schritt zu unterstützen.

Weitere Informationen finden Sie unter https://www.jnj.com/innovative-medicine

Wir suchen das beste Talent für die Position des/der Lead Specialist Maintenance Technician (m/w/d) in Schaffhausen.

Ihre Aufgaben & Verantwortlichkeiten:

  • Koordination und Optimierung der Instandhaltungsarbeiten von Produktionswaagen und Reinräumen.
  • Sicherstellung der Verfügbarkeit von Produktionswaagen, Reinräumen und Produktionsanlagen.
  • Koordinierung von Dienstleistern im Hinblick Kalibrierung von Waagen und Produktionsanlagen, sowie Qualifizierung von Reinräumen.
  • Mitwirkung in Projektteams bei der Anschaffung von neuem Equipment.
  • Mitwirkung in GMP Compliance Inspektionen als Subject Matter Expert (SME).
  • Durchführung von Qualifizierungsarbeiten im Rahmen von Projekten.
  • Vorbereitung und eigenverantwortliche Durchführung messtechnischer Überprüfungen in Reinräumen.
  • Störungsbehebung an Produktionsanlagen (Messtechnik) für die pharmazeutische Produktion.
  • Einhaltung der Sicherheits-, Hygiene-Umweltschutz- und GMP-Vorschriften (Good Manufacturing Practice).
  • Aktive Einbringung von Erfahrungen und Visionen durch eigene Ideen und Optimierungsvorschläge um einen wichtigen Beitrag zur kontinuierlichen Verbesserung unserer Produktionsanlagen, Instandhaltungsstrategien und Arbeitsabläufe zu leisten.

Ihr Qualifikationsportfolio & unsere Anforderungen:

  • Erfolgreich abgeschlossenes technisches Studium oder eine technische Weiterbildung z.B. Dipl. Systemtechniker, Dipl. Maschinenbautechniker.
  • Team orientiertes Arbeiten, Interdisziplinäre Zusammenarbeit.
  • Bereitschaft nach kontinuierlicher persönlicher Weiterentwicklung.
  • Zuverlässigkeit, Flexibilität und eine gute Selbstorganisation.
  • Sichere Anwendung von MS Office und Grundkenntnisse SAP.
  • Deutsch mündlich und schriftlich verhandlungssicher, sowie gute Englischkenntnisse.

Wünschenswert:

  • Erfahrungen in der Reinraum Messtechnik.
  • Erfahrung in einem Pharmazeutischen GMP, ISO, Explosionsschutz und EHS&S (Sicherheit, Gesundheits- und Umweltschutz) Umfeld.
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