QA Documentation Specialist

Lonza is seeking a QA Documentation Specialist to support GMP-compliant documentation for biopharmaceutical development and manufacturing. In this role, you will create, review, and maintain quality records, SOPs, batch documents, and change controls to ensure data integrity and regulatory compliance. You will collaborate with QA, manufacturing, and R&D teams to manage document workflows, support audits and inspections, and drive continuous improvement in document control processes. This positi…