Jobs 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.

The Senior Specialist is responsible for leading technical reviews, ensuring compliance, mentoring junior staff, and supporting quality investigations related to assays and technologies in a life sciences environment.

In this role, you will perform GMP manufacturing operations, handle equipment, maintain lab standards, and apply aseptic techniques in a team-oriented environment.

Lead technology transfer of manufacturing processes for cell & gene therapy while providing technical oversight during GMP runs and continuous improvements.

Perform timely testing and analysis of in-process and final product samples per SOPs and cGMP. Operate and troubleshoot HPLC and spectroscopy methods, document results, support method transfers/validation and equipment qualification, manage lab supplies, and contribute to continuous improvement activities.

As a Biotechnologist, you will perform GMP manufacturing operations, maintain facility standards, handle bioreactors, and utilize process control systems.

The Lead QA Specialist oversees daily Quality Assurance in a cGxP manufacturing facility, ensuring compliance with regulations, reviewing documentation, and leading investigations. This role requires collaboration with teams and participation in regulatory audits while mentoring staff and driving continuous improvement efforts.

As an Intern, you'll gain hands-on experience in pharmaceutical manufacturing, adhering to cGMP, and supporting daily operations while developing problem-solving skills.

Lead QC analyst responsible for biochemistry testing to support lot release: perform ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, potency and physicochemical assays; document results per cGMP and data integrity; troubleshoot, maintain equipment, support validations, OOS/deviation investigations, train staff, and author SOPs and change controls.

The Site HR Head leads HR activities aligning with business goals, manages talent development, employee relations, and team performance in Singapore.

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.

15-month on-the-job Attach & Train QC trainee role based at Lonza Tuas. Perform analytical testing (final product, in-process, raw material, environmental), document results under cGMP, maintain lab operations, support sample logistics, prepare reagents/standards, follow data integrity, and contribute to continuous improvement. Work rotating 12-hour day shifts.

Provide QA oversight for GMP biopharmaceutical manufacturing: review and approve SOPs, batch records, lead investigations (deviations, CAPA, change control), support audits/inspections, manage small projects, and train/audit internally to ensure regulatory compliance and batch disposition.

Perform microbiological and biochemical QC testing (bioburden, LAL, PCR, ELISA, flow cytometry, environmental monitoring, compendial tests), document results under cGMP, support method transfer/validation, equipment qualification and troubleshooting, investigate OOS/deviations, maintain lab supplies and housekeeping, and generate trending and reports.

15-month attached-and-trained GMP manufacturing trainee role based at Tuas. Perform equipment monitoring, basic lab sampling and measurements, sanitization, CIP/SIP tasks, aseptic handling, process troubleshooting, SOP and batch record use, and attain full competency across assigned manufacturing operations on rotating 12-hour shifts.

15-month on‑site trainee role supporting GMP-regulated pharmaceutical manufacturing. Perform supervised laboratory/manufacturing tasks, documentation, equipment monitoring, sample collection, and use LIMS/MES/ERP while learning quality systems, SOPs, and CAPA processes.

Support day-to-day GMP laboratory operations including buffer/media prep, equipment checks, environmental monitoring, documentation, coordination with teams, and continuous improvement initiatives while maintaining data integrity and EHS compliance.

Lead scientific process development for mammalian-cell biologics across upstream, downstream, characterization, and validation. Solve complex technical challenges using DoE, multivariate analysis, RCA, and risk-based approaches; support clinical and cGMP transfers, mentor teams, engage customers, and implement process improvements and emerging technologies to ensure robust, regulatory-compliant manufacturing.