We are looking for a QC-Analyst with hands-on experience in ELISA testing and Capillary Electrophoresis (CE) to support lot release activities within our Quality Control Biochemistry Laboratory.
This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. This is a 12-hour day shift role.
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
Perform biochemical testing to support lot release, in-process, stability, and final product testing.
Execute analytical methods including ELISA, Capillary Electrophoresis (CE), SDS-PAGE, PCR, IEF/icIEF, potency assays, and other physicochemical techniques.
Accurately document, review, and report test results in compliance with cGMP and data integrity requirements.
Prioritize testing activities to meet production and business timelines.
Prepare and maintain laboratory reagents, reference standards, and other materials required for testing.
Support routine laboratory operations, including equipment maintenance, qualification, troubleshooting, inventory management, and housekeeping.
Any other tasks as and when assigned by supervisor
What we’re looking for
Diploma or Degree in Life Sciences, Biotechnology, Chemistry, or a related discipline.
Experience in a biopharmaceutical QC laboratory supporting GMP operations.
Strong hands-on experience with ELISA testing and Capillary Electrophoresis (CE) is essential.
Familiarity with additional analytical techniques such as PCR, SDS-PAGE, IEF/icIEF, and potency assays is an advantage.
Good understanding of GMP, FDA, EMA, ICH guidelines, and data integrity principles.
Strong analytical, problem-solving, and communication skills, with the ability to work independently and collaboratively in a fast-paced laboratory environment.
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.
Lonza Singapore, Singapore, SGP Office
Singapore, Singapore
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