Lonza AG

QC Analyst / Data Reviewer

📍 CH - Visp

Rolle und Verantwortlichkeiten

You review HPLC data and other laboratory-related raw data to ensure accuracy, completeness, and compliance. You perform tasks within the gLIMS laboratory execution system, including creating consumable types and managing instruments and consumables. You ensure all activities comply with GMP requirements and internal procedures. You investigate ambiguous results with curiosity and attention to detail. You adapt effectively to changing priorities in a dynamic Quality Control environment.

Team / Beschreibung

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 for all employees.

Qualifikationen und Fähigkeiten

  • You have completed training as a laboratory technician or hold a bachelor’s degree in chemistry, biochemistry, or a related scientific field.

  • Experience in a GMP-regulated Quality Control environment is highly preferred.

  • Hands-on experience with HPLC and/or capillary electrophoresis (CE) is preferred.

  • You bring a highly detail-oriented, flexible, and investigative mindset.

  • You communicate fluently in English; German skills are a plus.