QC Associate, Analyst

The QC Associate, Analyst position is with Lonza, a worldwide leader in life‑science manufacturing, located at the state‑of‑the‑art Visp site in Switzerland. In this role you will carry out routine quality‑control testing and analytical release of raw materials, intermediates and finished products. Daily work involves executing validated methods, operating and maintaining chromatographic instruments such as HPLC and GC, and entering results in compliance with cGMP and ISO documentation standards. You will also support the investigation of out‑of‑specification findings, ensuring that any deviations are recorded, analysed and resolved according to internal procedures. The ideal candidate holds a B.Sc. or M.Sc. in Chemistry, Pharmacy or a closely related discipline and brings at least two years of hands‑on QC laboratory experience. Proficiency with HPLC and GC, strong documentation skills, and a solid understanding of data‑integrity practices are essential. Working at Lonza's Visp facility provides exposure to a diverse product portfolio and the chance to contribute directly to products that improve patients' lives, within a globally recognised organisation. What the role asks for: - B.Sc. or M.Sc. in Chemistry, Pharmacy or related field - Minimum 2 years QC laboratory experience - Proficiency with HPLC chromatography - Proficiency with GC chromatography - Strong documentation skills under cGMP/ISO - Knowledge of data‑integrity practices