About the role
As a Batch Record Reviewer at Lonza, you will ensure that biopharmaceutical manufacturing batches meet the highest standards of quality, accuracy, and regulatory compliance. You will perform detailed cGMP reviews of batch production records, verify calculations and critical parameters, and identify documentation gaps or discrepancies. Partnering closely with manufacturing, QA, and validation teams, you will help resolve issues, support investigations and CAPAs, and maintain audit-ready document…