Batch Record Reviewer - cGMP Expert, Flexible Hours

Lonza • stalden (vs), wallis • Posted June 09, 2026

About the Role

Lonza in Visp is seeking a dedicated Batch Record Reviewer (80 - 100%) to join their team. The role involves planning and documenting manufacturing campaigns for drug products while ensuring compliance with GMPs and quality requirements.

The ideal candidate will have a background in Pharmaceutical Technology or related fields, with experience in sterile manufacturing and a strong command of German and English. Flexible working hours are part of the job.

#J-18808-Ljbffr