Jobs at Lonza

Support the HRBP team at the Tuas manufacturing site by managing complex employee relations cases, conducting investigations, coordinating medical/return-to-work cases, advising managers on risk-based solutions, ensuring compliance with Singapore employment law, supporting onboarding and engagement, and analyzing HR data to produce insights and recommendations.

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.

Site-based internship supporting Manufacturing Science and Technology (MSAT) in fill-and-finish pharmaceutical operations. Learn processes, ensure cGMP compliance, assist documentation and SOP development, troubleshoot process issues, and receive daily supervision and coaching in a quality-focused manufacturing environment.

Develop and revise Master Batch Records (MBRs), SOPs and Work Instructions to cGMP standards; manage document lifecycle, track changes, respond to reviewers, support change requests and CAPA closure, and produce aseptic process simulation reports while collaborating with SMEs to meet production schedules.

Trainee Biotechnologist enrolled in a 15-month attached-and-train program to learn GMP manufacturing of therapeutic proteins. Responsibilities include performing defined GMP procedures, cleanroom work, sampling and basic lab measurements, equipment setup and sanitization, CIP/SIP execution, aseptic technique, LIMS sample submission, and basic troubleshooting. Trainee will attain competency across assigned manufacturing operations and follow SOPs, batch records, and performance measures under supervision.

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

The Biotechnologist Trainee will perform GMP manufacturing tasks, including equipment monitoring, basic laboratory procedures, and maintaining cleanroom standards while working under supervision.

Support day-to-day QA activities for a multi-product GMP biotech contract manufacturing site. Oversee compliance with SOPs, cGxP/cGDP/GMP standards, lead complex quality projects, guide staff on corrective actions, participate in policy making, and communicate quality strategy to senior management while driving global harmonization and efficiency.

Provide QA oversight for process validation and ongoing process verification in a GMP biopharmaceutical site. Review and approve VMPs, protocols, reports, deviations, CAPAs and CPV documentation. Ensure validation execution aligns with approved protocols, SOPs, regulatory standards, Lonza policies and customer expectations. Support root cause investigations and timely closure of corrective actions.

Lead and supervise electrical engineers and technicians to perform maintenance, troubleshooting, repairs, and preventive maintenance in a cGMP manufacturing environment. Manage electrical and fire alarm systems, supervise vendors, ensure GMP/EHS compliance, train staff, and lead root cause analyses to minimize production disruption.

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.

The QA Specialist ensures compliance with GMP standards in manufacturing, reviews quality documents, leads investigations, and manages relationships with teams and partners.

The trainee will receive structured on-the-job training in technology transfer, document management, and collaboration with project engineers in the biopharmaceutical industry.

Perform biochemical and analytical testing (ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, potency assays, Biacore) for final, in-process, and stability samples under cGMP. Support method transfers/validations, equipment qualification, troubleshooting, investigations (OOS/deviations), and documentation (SOPs, change controls). Contribute to continuous improvement, reagent prep, equipment maintenance, and technical training.

Perform biochemical and analytical testing (ELISA, PCR, CE, SDS-PAGE, IEF, icIEF, Biacore, potency assays) on final, in-process, and stability samples under cGMP. Support method transfers, validations, equipment qualification, troubleshoot assays/equipment, investigate OOS and deviations, author quality documentation, and contribute to continuous improvement in a GMP-regulated biopharmaceutical QC laboratory.

The Senior Process Engineer will oversee technology transfer, process optimization, compliance, and documentation in the CGT division, ensuring GMP standards and collaborating with teams and clients.

The Principal Expert leads the data science strategy for MSAT, establishes best practices, delivers high-impact initiatives, and mentors teams in a regulated environment.

Support technical transfer and process-scale up of customer cell and gene therapy manufacturing into the Lonza Singapore facility. Design and run scale-down experiments, review batch records and SOPs, investigate deviations, implement change controls, support pre-campaign and on-floor oversight, and assist with audits and documentation. Work cross-functionally with customers, vendors, and internal teams while following lab safety and cGMP.

The Biotechnologist Trainee will learn to perform procedures in a GMP setting, monitoring equipment, conducting basic lab tasks, ensuring facility standards, and developing process expertise.

Lonza seeks fresh graduates in Life Sciences or related fields for various roles, emphasizing problem-solving, communication, and teamwork skills.