QC Analyst (Product Testing - Shift)

About the role

Lonza is hiring a QC Analyst in Tuas to perform timely testing and analysis of in-process and final product samples in compliance with SOPs and cGMP, ensuring accurate documentation and data integrity. The role supports lab operations, sample logistics and analytical methods such as HPLC and spectroscopy, and contributes to continuous improvement initiatives. It is a shift position.

Key responsibilities

• Prioritize and perform testing and analysis in a timely way to support business needs
• Analyse bulk, in-process and stability samples according to SOPs and test methods
• Document results in line with cGMP
• Troubleshoot analytical methods and equipment problems
• Take part in method transfers and validation, and in equipment qualification
• Help select QC equipment, standards and reagents
• Carry out assay trend analysis and document revisions
• Support general lab work: housekeeping, equipment maintenance, supply inventory and ordering, glassware management

Required profile

• Degree or diploma in Chemistry, Science or equivalent
• Relevant work experience, preferably lab experience in a biotech or medically related field
• Willingness to work 12-hour rotating shifts

Required skills

• Good understanding of HPLC, CE, TOC, osmolality and protein concentration methods (A280 or SoloVPE)
• Empower software
• Spectroscopy and other assigned methods, including chromatography

What we offer

• Competitive compensation programs for high performers
• Comprehensive medical insurance with family coverage at partially subsidised premiums
• Company transport from designated MRT stations to and from the Tuas site
• Cross-functional projects and global exposure for professional growth