Teams at Lonza

Perform analytical testing on therapeutic protein samples (HPLC, capillary electrophoresis, spectrophotometry), review and interpret data against specifications, prepare stability study protocols and reports, support investigations/CAPAs/change controls, mentor colleagues, manage lab operations, and collaborate with QC/QA/Manufacturing to ensure GMP compliance and product quality.

Lead MSAT process readiness for a U.S. bioconjugate drug substance growth project. Own process implementation through design, commissioning, qualification, validation, start-up, technology transfer, and operational handover. Coordinate cross-functional teams, manage risks, build an MSAT operations team, and ensure GMP compliance and long-term manufacturing excellence.

Design, implement, and maintain control systems and instrumentation for biopharmaceutical manufacturing. Configure and troubleshoot PLCs, DCS (Emerson DeltaV), SCADA/HMI; support commissioning, validation, calibration, root-cause investigations, documentation, and cross-functional collaboration to ensure compliant, reliable production.