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.

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.

Lead technology transfer of cell and gene therapy processes into site, design and run scale-down studies, provide on-floor GMP oversight, troubleshoot deviations, monitor process performance, author process and quality documentation, and support audits, inspections and plant start-up activities while partnering cross-functionally to enable clinical and commercial manufacturing.

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.

Perform biochemical and physicochemical testing (ELISA, CE, SDS-PAGE, PCR, IEF/icIEF, potency assays) to support lot release, in-process, stability, and final product testing. Document and report results per cGMP and data integrity, maintain reagents and equipment, troubleshoot, support inventory and lab operations, and prioritize testing to meet production timelines.

15-month Attach-and-Train QC trainee role performing on-site analytical testing of final product, in-process, raw material and environmental samples per SOPs and cGMP. Duties include spectroscopy and chromatography methods (HPLC, TOC, A280/SoloVPE), documentation, lab maintenance, sample logistics, reagent preparation, data integrity, and continuous improvement. Rotating 12-hour day/night shifts at Tuas site.

Lead new customer acquisition across APAC for Lonza, building relationships from technical staff to C-suite, developing territory and value proposition strategies, identifying market trends, and driving high-value CDMO deal revenue and pipeline growth.

Lead cross-functional program teams to deliver projects on quality, timeline, and cost. Serve as primary customer interface, ensure adherence to global PPM standards, maintain data integrity (including Planview), and drive stakeholder satisfaction throughout program lifecycle.

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.

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.

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.