Auf einen Blick
- Aufgaben: Sichere den Betrieb von kleinen Fertigungsgeräten und unterstütze die Produktion lebensverändernder Biopharmazeutika.
- Unternehmen: Innovatives Unternehmen im Bereich Biopharmazeutika mit einer dynamischen Arbeitskultur.
- Vorteile: Agile Karriere, inklusive Arbeitsumgebung und spannende Herausforderungen.
- Weitere Informationen: Engagiertes Team mit Möglichkeiten zur persönlichen und beruflichen Weiterentwicklung.
- Warum dieser Job: Gestalte die Zukunft der Lebenswissenschaften und arbeite an bedeutenden Projekten.
- Qualifikationen: Mindestens 10 Jahre Erfahrung in der Ingenieurwissenschaft, idealerweise in der Pharmaindustrie.
Das prognostizierte Gehalt liegt zwischen 63000 - 77000 CHF pro Jahr.
Production Engineer
Production Engineer - Small Devices
Ensure the operational readiness and reliability of vital small manufacturing equipment at our Bio Atrium facility in Visp, directly supporting the delivery of life-changing biopharmaceuticals.
This is a fully site-based 6-month contract role.
Fully site‑based roles
This is a fully site‑based role.
Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
What you will do:
Drive equipment lifecycle management and reliability for small utility and process devices across the Bio Atrium site.
Support the continuous production of biopharmaceuticals by minimizing equipment downtime through proactive preventive and corrective maintenance.
Serve as the Subject
Expert (SME) on CAPEX projects, contributing to equipment design, selection, procurement, installation, and commissioning.
Collaborate closely with cross-functional teams including Engineering, Operations, Quality, and Validation to maintain operational excellence.
Troubleshoot complex equipment deviations using structured Root Cause Analysis (RCA) and implement effective CAPAs.
Author, review, and manage critical c GMP documentation, including SOPs, work instructions, change controls, and investigation reports.
Represent the engineering department during internal and external audits, ensuring complete audit readiness for small device systems.
What we are looking for:
Minimum 10 years of professional engineering experience, with at least 3 years in a c GMP pharmaceutical or biotechnology manufacturing environment.
Proven expertise in equipment lifecycle management, reliability engineering, and maintenance optimization.
Hands-on experience with equipment commissioning, qualification, and validation (CQV/Validation: IV, IQ/OQ/PQ) and risk assessments.
Demonstrated track record in technical troubleshooting and Root Cause Analysis (RCA); formal RCA certification is an advantage.
Strong proficiency in authoring and managing GMP quality records (deviations, CAPAs, change controls).
Professional fluency in English (written and spoken); working knowledge of German is an advantage.
Degree in Engineering (Mechanical, Process, Chemical, or related technical discipline).
About Lonza
At Lonza, our people are our greatest strength.
With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow.
Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together.
Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table.
At Lonza, we value diversity and are committed to creating an inclusive environment.
As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.
Ready to play your part in shaping the future of life sciences?
Apply now. jid5c3d9a3ws jit0936ws jiy26ws
Production Engineer Arbeitgeber: Lonza Group AG
Lonza ist ein hervorragender Arbeitgeber, der eine dynamische Arbeitskultur und agile Karrieremöglichkeiten in einem hochmodernen biopharmazeutischen Umfeld bietet. In Visp, Schweiz, profitieren Mitarbeitende von einer inklusiven und ethischen Arbeitsumgebung, die enge Zusammenarbeit und persönliche Entwicklung fördert. Hier haben Sie die Möglichkeit, direkt zur Qualitätssicherung lebensrettender Therapien beizutragen und Ihre beruflichen Fähigkeiten in einem unterstützenden Team weiterzuentwickeln.
