Analyst, QC (BioChemistry)

Responsibilities

• Perform and prioritize testing of final product, in-process, and stability samples in accordance with approved test methods, SOPs, and cGMP requirements.
• Execute biochemical and analytical methods including ELISA, PCR, CE, SDS-PAGE, IEF, icIEF, potency assays, Biacore, and other physiochemical techniques.
• Support method transfers, method validations, equipment qualification activities, and laboratory troubleshooting to ensure operational readiness and compliance.
• Document, review, and maintain laboratory data and records in accordance with GMP requirements and data integrity principles.
• Investigate laboratory events including OOS, deviations, and analytical issues, supporting root cause analysis and technical report generation.
• Author and maintain quality documentation including Change Controls, SOPs, test methods, and laboratory procedures.
• Contribute to continuous improvement initiatives, laboratory operations, equipment maintenance, reagent preparation, and technical training activities.

Requirements

• Degree, or higher qualification in Biochemistry, Biotechnology, Life Sciences, Pharmaceutical Sciences, Chemistry, or a related discipline.
• At least 5 years of Quality Control or laboratory experience within the biopharmaceutical, biotechnology, or pharmaceutical industry.
• Hands-on experience with biochemical and analytical techniques such as ELISA, PCR, CE, SDS-PAGE, IEF, icIEF, potency assays, and Biacore.
• Experience supporting method transfers, method validations, equipment qualification, and laboratory investigations.
• Good understanding of cGMP requirements, quality management systems, data integrity principles, and global regulatory expectations including FDA, EMA, and ICH guidelines.
• Strong analytical, troubleshooting, problem-solving, and quality decision-making skills with the ability to work independently and prioritize effectively.
• Strong communication and interpersonal skills with a collaborative mindset and commitment to safety, quality, and operational excellence.
• About Lonza
• Ready to shape the future of life sciences?

Additional Information

Location: Tuas, Singapore Join Lonza's Quality Control team and play a critical role in ensuring the quality, safety, and compliance of biopharmaceutical products that improve lives around the world. As a QC Analyst, Biochemistry, you will perform analytical testing, support method transfers and validations, troubleshoot laboratory methods and equipment, and contribute to continuous improvement initiatives within a GMP-regulated environment. This role offers the opportunity to work with advanced analytical techniques while supporting the manufacture and release of life-changing therapies. What you will get - An agile career and dynamic working culture. - An inclusive and ethical workplace. - Compensation programs that recognize high performance. - Opportunities to collaborate with global cross-functional teams. - Ongoing learning and professional development opportunities. - Our full list of global benefits can be found here: Lonza Benefits .

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