Senior QC Biochemistry Analyst – Lot Release

Lonza Biologics Tuas Pte Ltd; Singapore; On-site; Confidential; Full time

Benefits offered by this job

Medical insurance

Transport provided

Career growth

Global exposure

Benefits portal

Job summary

Lonza Biologics Tuas Pte Ltd is seeking a QC Analyst to support the Biochemistry area in Lot Release activities. You will prioritize and perform analytical testing, including ELISA, PCR, CE, SDS-PAGE and IEF/icIEF, while ensuring data integrity and GMP compliance.

The role requires a degree and about 5 years of QC/quality experience in biopharmaceuticals, with strong documentation, planning, and communication skills. On-site in Singapore with comprehensive benefits and transport support.

Qualifications

• 5 years of experience in QC/Quality within biopharmaceuticals.
• Familiarity with FDA/EMEA/ICH guidelines and GMP systems.
• Strong planning, documentation, and data integrity practices.

Responsibilities

• Prioritize and perform analytical testing to meet business timelines.
• Test final product, in-process, and stability samples per SOPs.
• Document and review results in compliance with cGMP and data integrity requirements.
• Execute ELISA, PCR, CE, SDS-PAGE, IEF/icIEF and related assays.
• Support general lab operations: housekeeping, equipment upkeep, inventory, autoclaving.
• Prepare and maintain standards/reagents per GMP.
• Troubleshoot analytical methods and equipment issues.
• Participate in equipment qualification and maintenance.
• Assist or lead OOS and deviation investigations; draft reports.
• Train others on test methods and contribute to method transfer.
• Author change controls, test methods, and SOPs.

Skills

QC/Quality experience

Biopharmaceuticals

Documentation skills

GMP knowledge

Lab testing

Education

Bachelor's degree

Tools

ELISA

PCR

CE

SDS-PAGE

IEF/icIEF

Job description

Lonza Biologics Tuas Pte Ltd is seeking a QC Analyst to support the Biochemistry area in Lot Release activities. You will prioritize and perform analytical testing, including ELISA, PCR, CE, SDS-PAGE and IEF/icIEF, while ensuring data integrity and GMP compliance.

The role requires a degree and about 5 years of QC/quality experience in biopharmaceuticals, with strong documentation, planning, and communication skills. On-site in Singapore with comprehensive benefits and transport support.