Senior QA Lead – Biopharma cGMP Projects

Lonza is seeking a Senior QA Specialist for QA Projects based in Visp, Switzerland. The role entails owning quality responsibilities for biopharmaceutical manufacturing, ensuring compliance with cGMP standards, and managing project timelines.

Candidates should hold an academic degree in chemistry or related fields with solid experience in the GMP-regulated pharmaceutical industry. The position includes training junior employees and involves strong communication skills to interact with health authorities.

Relocation assistance is available for eligible candidates.