Senior QA Specialist — Biopharma cGMP Project Lead (Visp)

Lonza is seeking a Senior QA Specialist in Visp, Switzerland. In this role, you will oversee quality responsibilities for manufacturing biopharmaceutical products. You will ensure compliance with GMP standards, review critical documentation, and lead investigations for quality issues.

The ideal candidate holds a degree in Chemistry or related fields and has solid experience in the pharmaceutical industry. You will also mentor junior staff, driving quality assurance and compliance initiatives across projects at Lonza.