Jobs at Lonza

Pharmaceutical manufacturing intern supporting fill-and-finish operations across manufacturing, quality, development, and MSAT teams. Responsibilities include learning pharmaceutical processes, following cGMP and safety requirements, developing procedures, troubleshooting process issues, organizing documentation, and supporting day-to-day site operations under supervision.

Supports downstream purification development for recombinant protein therapeutics. Performs chromatography, filtration, viral clearance, sampling, testing, and data collection; prepares buffers and reagents; operates purification equipment; assists with technology transfer, process optimization, and characterization studies; troubleshoots experimental issues; and maintains EHS, quality, cGMP, and data integrity compliance in a site-based laboratory.

Manufactures therapeutic proteins under cGMP conditions in cleanroom environments. Performs equipment monitoring, laboratory sampling, sanitization, aseptic handling, equipment preparation and operation, CIP/SIP activities, troubleshooting, materials and solutions preparation, and process documentation. Uses SOPs, logbooks, batch records, and LIMS while developing competency in biopharmaceutical manufacturing operations through a 15-month structured training program.

Leads purification process development and characterization for recombinant protein manufacturing, including chromatography, UF/DF, viral clearance, scale-down models, DoE, risk assessments, and resin lifetime studies. Provides scientific leadership, technical supervision, regulatory and manufacturing support, troubleshooting, technology transfer assistance, and customer communication. Trains junior scientists, reviews technical documentation, coordinates multiple projects, and drives safety and operational improvements.

Conduct analytical testing and protein characterization studies using mass spectrometry, chromatography, electrophoresis, and related methods. Analyze and interpret data, support reference standard qualification, forced degradation, product characterization, and biocompatibility studies under ICH and cGMP guidelines. Review GMP documentation, maintain laboratory equipment and inventory, troubleshoot issues, support safety and training programs, and contribute to automation and operational improvements.

Provides day-to-day QA support for a biopharmaceutical manufacturing facility, reviewing and approving GMP documentation, deviations, investigations, CAPAs, change controls, validation activities, and quality events. The role supports audits, data integrity, process improvements, changeovers, and risk-based quality decisions. It leads small projects, coordinates cross-functional activities, trains and guides junior QA staff, and provides QA oversight for operational and process changes.

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.

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.

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.

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.

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 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 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.