About the role
As a QMS Administrator at Lonza, you will own day-to-day operation of our electronic Quality Management System supporting advanced biopharmaceutical development and manufacturing. You will configure and maintain QMS workflows, manage documentation and records, and support deviation, CAPA, and change control processes in a highly regulated GMP environment. Partnering with QA, manufacturing, engineering, and IT, you will ensure data integrity, prepare quality metrics and reports, and train users …