Senior QC Analyst – Biochemistry & Methods

Lonza; Singapore; On-site; Confidential; Full time

Benefits offered by this job

Medical insurance

Company transport from designated MRTs

Professional growth opportunities

Job summary

Lonza Singapore is seeking a Lead Analyst in Quality Control (Product Testing) to support Lot Release activities in Biochemistry, with hands-on analytical testing and method execution.

You will perform ELISA, PCR, CE, SDS-PAGE, and other assays, ensure GMP compliance, document results, participate in validations, OOS investigations, and training, within a collaborative, fast-paced environment. The role offers professional growth, cross-functional exposure, and a safety-focused culture.

Qualifications

• Degree or higher in biochemistry/quality-related field with 5+ years QC experience in biopharma.
• Lab experience in biotech/healthcare settings is preferred.
• Familiarity with FDA/EMEA/ICH guidelines and GMP systems.
• Strong planning, documentation, and interpersonal skills.

Responsibilities

• Prioritize and perform analytical testing to meet timelines.
• Test final product, in-process, and stability samples per SOPs.
• Document and review results in compliance with cGMP and data integrity.
• Execute methods such as ELISA, PCR, CE, SDS-PAGE, and related assays.
• Support general lab operations, equipment upkeep, inventory, autoclaving.
• Prepare standards/reagents and troubleshoot assay/equipment issues.
• Participate in equipment qualification/maintenance and OOS investigations.
• Draft reports, change controls, test methods, and SOPs; train others.

Skills

QC knowledge

Biopharmaceutical experience

Analytical testing

Documentation

Communication

Education

Bachelor's degree in Biochemistry/Quality

Tools

ELISA

PCR

CE

SDS-PAGE

IEF/icIEF

Job description

Lonza Singapore is seeking a Lead Analyst in Quality Control (Product Testing) to support Lot Release activities in Biochemistry, with hands-on analytical testing and method execution.

You will perform ELISA, PCR, CE, SDS-PAGE, and other assays, ensure GMP compliance, document results, participate in validations, OOS investigations, and training, within a collaborative, fast-paced environment. The role offers professional growth, cross-functional exposure, and a safety-focused culture.