QC Analyst / Data Reviewer

Lonza Visp, Valais – Suisse Publié le 24/09/2026
Description du poste
Overview

In this role, you support timely monoclonal antibody release by reviewing QC data and ensuring GMP-aligned analysis in the Visp lab. You work with HPLC and capillary electrophoresis data, verify accuracy in the gLIMS system, and help drive data integrity in a dynamic, cross-functional environment. You will collaborate with a diverse team to sustain quality and continuous improvement in analytical QC. This is an opportunity to contribute to impactful therapies within a modern, technology-forward lab.

Leistungen / Benefits
  • Agile scientific career in GMP environment
  • Inclusive workplace
  • Compensation programs recognizing performance and expertise
  • Opportunities to own impactful projects
  • Exposure to cross-functional collaboration
  • Competitive local benefits
Verantwortungsbereiche
  • Review HPLC data and other raw data for accuracy, completeness, and compliance
  • Operate within the gLIMS system, including creating consumable types and managing instruments
  • Ensure activities comply with GMP requirements and internal SOPs
  • Investigate ambiguous results with attention to detail
  • Adapt to changing priorities in a dynamic QC environment
Zentrale Anforderungen
  • Laboratory technician training or bachelor’s degree in chemistry, biochemistry, or related field
  • Experience in GMP-regulated QC environment preferred
  • Hands-on experience with HPLC and/or capillary electrophoresis preferred
  • Detail-oriented, flexible, investigative mindset
  • Fluent in English; German a plus
  • attention to detail
  • curiosity and investigative mindset
  • flexibility and adaptability
  • HPLC
  • capillary electrophoresis (CE)
  • GMP compliance
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