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Lonza

Lead Analyst, Quality Control (Chromatography)

SG - Tuas, Singapore

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hirly's read of this role

Seniority
Lead / management
Country
SG
Work mode
On-site / unstated
First seen by hirly
27 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

The QC Analyst will be responsible for Biochemistry Area in the QC Lab to support Lot Release activities

What you’ll get

An agile career and dynamic working culture in a global life sciences leader.

An inclusive and ethical workplace that values diversity and integrity.

Competitive compensation programs that recognize high performance.

Professional growth opportunities through cross-functional projects and global exposure.

Comprehensive medical insurance, with the option to enroll family members at partially subsidized premiums.

Company transport provided from designated MRT locations to and from the Tuas site.

Access to Lonza’s full suite of employee benefits: www.lonza.com/careers/benefits

What you’ll do:

Prioritize and perform analytical testing to meet business timelines

Test final product, in-process, and stability samples per SOPs and methods

Document and review results in compliance with cGMP and data integrity requirements

Execute methods such as ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, potency, and other physicochemical assays

Support general lab operations: housekeeping, equipment upkeep, inventory, autoclaving, and glassware management

Prepare and maintain standards/reagents based on GMP requirements

Troubleshoot analytical methods and equipment issues

Participate in equipment qualification and maintenance

Support or lead OOS and deviation investigations; draft reports

Train others on test methods

Contribute to method transfer and validation activities

Author change controls, test methods, and SOPs

What we’re looking for:

Degree or higher with 5 years of QC/Quality experience in biopharmaceuticals

Preferably lab experience in biotech or medically related fields

Familiarity with FDA, EMEA, ICH guidelines and GMP quality systems

Strong planning, prioritization, and documentation skills

Good communication and interpersonal abilities

Analytical, meticulous, and quality-focused mindset

Team player who can work independently with strong safety and timeline discipline

Openness to new challenges and continuous improvement

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

Original posting on Lonza's site ↗

Listed on hirly, a job board. hirly is not the employer: Lonza is hiring for this role.

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