Production Engineer

Lonza Group AG

Eyholz

Vor Ort

CHF 110.000 - 150.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden
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Zusammenfassung

Lonza Group AG is seeking a Production Engineer to drive equipment lifecycle management and reliability for small utility and process devices at the BioAtrium site. The role emphasizes proactive maintenance to minimize downtime and ensure continuous biopharmaceutical production.

You will serve as SME on CAPEX projects, collaborating across Engineering, Operations, Quality and Validation. Candidates should have deep experience with CQV/Validation (IV, IQ/OQ/PQ) and risk assessments, and a strong

Qualifikationen

  • 10+ years of professional engineering experience, incl. 3+ years in a cGMP pharmaceutical or biotechnology manufacturing environment.

Aufgaben

  • Drive equipment lifecycle management and reliability for small utility and process devices at BioAtrium.
  • Support continuous production by minimizing equipment downtime through preventive and corrective maintenance.
  • Serve as SME on CAPEX projects, contributing to equipment design, selection, procurement, installation, and commissioning.
  • Collaborate with Engineering, Operations, Quality, and Validation to maintain operational excellence.
  • Troubleshoot complex equipment deviations using RCA and implement CAPAs.
  • Author, review, and manage cGMP documentation, including SOPs, work instructions, change controls, and investigation reports.
  • Represent the engineering department during audits and ensure audit readiness for small device systems.

Kenntnisse

Equipment lifecycle management
Reliability engineering
Maintenance optimization
CQV/Validation
Root Cause Analysis
GMP documentation
Audit readiness
English language
German language (advantage)

Ausbildung

Engineering degree (Mechanical/Process/Chemical)

Jobbeschreibung

Production Engineer

Lonza Group AG Vacant since : 04.09.2026 3930 Eyholz (VS) 90% - 100% By agreement Temporary

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 BioAtrium 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 cGMP 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 cGMP 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.

Work location & details
  • Work location 3930 Eyholz (VS)
  • Workload 90% - 100%
  • Employment start By agreement
  • Employment duration Temporary
  • By online Online form
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