Jobs at Lonza

Lead QA Audit Specialist to support audit activities and GMP/cGxP compliance at a multi-product contract manufacturing site. Responsibilities include internal GxP auditing, inspection and customer audit support, audit walkdown preparation, audit/inspection responses, leading complex deviation investigations, owning assigned quality process documents, and serving as subject-matter expert and trainer.

Supports audit management and quality assurance activities at a cGxP contract manufacturing facility. Responsibilities include developing internal GxP auditing skills, supporting regulatory inspections and customer audits, preparing audit walkdowns, leading audit and inspection responses, managing complex deviation investigations, owning quality-process documents, becoming a qualified trainer, and serving as a subject matter expert. The role requires practical QA operations experience in a GMP-regulated biopharmaceutical environment and strong knowledge of quality systems and regulatory guidelines.

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.

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.

Performs biochemistry QC testing for lot release, final products, in-process and stability samples. Maintains GMP documentation and laboratory operations, troubleshoots methods and equipment, supports investigations, qualifications, validation and method transfers, and authors SOPs, test methods and change controls. The role also trains colleagues and ensures testing meets quality, safety and business timelines.

Perform timely testing and analysis of in-process and final product samples per SOPs and cGMP. Support lab operations, sample logistics, analytical methods (HPLC, CE, spectroscopy), troubleshoot equipment, assist method transfers and validation, qualify/maintain QC equipment, analyze assay trends, manage lab inventory and housekeeping, and work 12-hour rotating shifts.

Support cGMP biopharmaceutical manufacturing by preparing materials, equipment and cleanroom areas. Perform sanitization, sampling (pH, conductivity, osmolality), execute SOPs and batch records, use LIMS, develop DeltaV competency, support quality/compliance activities, and collaborate with cross-functional teams while working rotating 12-hour shifts.

Perform biochemical and analytical testing (ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, Biacore, potency assays) for final, in-process, and stability samples under cGMP. Support method transfers and validations, equipment qualification, investigations (OOS/deviations), documentation (SOPs, Change Controls), and continuous improvement in a GMP-regulated QC laboratory.

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.

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.

15-month site-based trainee role to learn and perform cGMP biomanufacturing of therapeutic proteins. Tasks include following SOPs, documenting data, reporting deviations, handling materials/equipment in cleanrooms, supporting housekeeping and training, and upholding data integrity and safety.

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.

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.

Support day-to-day Quality Assurance activities at a cGxP contract manufacturing facility: manage GMP documentation lifecycle, issue controlled documents, assist in inspections and audits, perform material release inspections, detect and correct cGxP/cGDP non-compliance, and uphold data integrity.

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 and deliver customer programs in a life-sciences/CDMO environment. Build trusted customer relationships, manage cross-functional teams, ensure quality, timelines, cost, and adherence to PPM CoE standards and data integrity (Planview). Drive continuous improvement and represent customer interests on-site.