Teams at Lonza

Lead QA Specialist responsible for daily QA in a multi-product cGxP manufacturing site: reviewing/approving batch records and quality documentation, leading investigations and CAPAs, supporting batch disposition and audits, driving data integrity, mentoring staff, and ensuring GMP compliance on a rotating 12-hour onsite shift.

Perform complex cGMP release testing (flow cytometry, ELISA, PCR, cell culture), lead method transfers and validations, review lab data, lead OOS investigations, manage CAPA/change controls, author SOPs, and train junior QC staff to ensure compliant product release.

Receive, verify, and document incoming materials; perform SAP transactions and RF scanning; inspect and put away inventory; operate forklifts and pallet jacks; support cross-training across shipping, warehouse, and kitting while maintaining cGMP compliance and audit-ready records.