Teams at Lonza

Support cGMP manufacturing of therapeutic proteins at Tuas site by operating and troubleshooting equipment, performing aseptic techniques, sampling, documentation (Batch Records, LIMS, DeltaV), ensuring data integrity, collaborating with MSAT/Engineering/Quality, maintaining training compliance, and contributing to continuous improvement and production schedules.

Lead QA oversight for cGxP manufacturing and associated functions. Provide technical leadership on deviations, CAPAs, change control, investigations, documentation review, inspections and audits. Drive cross-functional quality improvements, support regulatory readiness, mentor junior staff, and ensure product quality, data integrity and compliance with Lonza quality standards and regulatory requirements.

Perform and oversee GMP laboratory testing, support method transfers and validations, lead OOS/deviation investigations, author and maintain QC documentation, train staff, and drive continuous improvement and data integrity in a pharmaceutical/biotech QC environment.