Jobs at Lonza

Manages customer-facing scientific programs for bioscience products, translating client needs into execution plans and coordinating cross-functional delivery. Oversees contractual obligations, client relationships, risks, escalations, media development, non-GMP pilot activities, product supply, forecasting, client visits, and business reviews. Supports regional testing clients and new system installations while maintaining demand signals through SAP IBP. Requires life sciences or equivalent experience, FDA-regulated biotech or pharma experience, CDMO knowledge, strong communication skills, and project or client management expertise.

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.

Performs material and equipment preparation for cGMP biopharmaceutical manufacturing. Maintains cleanrooms, sanitizes equipment, conducts basic laboratory measurements, executes SOPs and batch records, submits samples through LIMS, and supports quality, validation, environmental monitoring, deviations, and data integrity activities. Collaborates with Manufacturing, MSAT, and QA teams while working rotating 12-hour shifts in a cleanroom environment.

Leads MSAT purification process support at Lonza’s Singapore manufacturing facility, including process monitoring, investigations, deviation closeout, batch-record review, change implementation, GMP and commercial runs, and process improvements. Maintains process databases, supports APR and CPV reporting, BLA filings, audits, and inspections. Provides technical mentorship, operator training, and cross-functional support while ensuring data integrity and batch-to-batch consistency.

Conduct analytical testing of antibodies and recombinant proteins using methods including capillary electrophoresis, HPLC/UPLC, qPCR, ELISA, and oligosaccharide profiling. Operate automated high-throughput laboratory platforms, troubleshoot and optimize methods, interpret experimental results, document methods and study reports, investigate atypical results, and support process development and regulatory submissions. The role requires scientific laboratory expertise and understanding of recombinant protein production, purification, analysis, and cGMP expectations.

Perform analytical testing of antibodies and recombinant proteins using capillary electrophoresis, HPLC/UPLC, qPCR, ELISA, oligosaccharide profiling, and automated high-throughput platforms. Troubleshoot and optimize methods, interpret experimental results, document methods and study reports, investigate atypical results, and support process development studies and IND/BLA applications while meeting regulatory and quality expectations.

Participate in a 15-month structured training program focused on small-scale downstream purification of biologics. Perform laboratory work using chromatography, ultrafiltration, and filtration systems under GMP standards. Generate and review scientific data, prepare inspection-ready records, support customer projects, coordinate project workstages, and communicate with local and global teams.

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.

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.

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.

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.

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.