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Lonza Group AG

Production Engineer - Small Devices

  • 3930 Visp
  • 80-100%
Jetzt bewerben

Ensure the operational readiness and reliability of vital small manufacturing equipment at the BioAtrium facility in Visp, directly supporting the delivery of life-changing biopharmaceuticals. This is a fully site-based 6-month contract 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.

Your tasks

  • 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 Matter 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 you bring

  • 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).

What the company offers

  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Competitive hourly rate.

About the company

At Lonza, people are the greatest strength. With over 30 sites across five continents, globally connected teams work together every day to manufacture the medicines of tomorrow. Lonza values diversity and is committed to creating an inclusive environment.