The QC Analyst will be responsible for performing a wide range of testing activities and role plays a key part in maintaining cGMP compliance through accurate documentation,
Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.
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. Normal working hours apply; however, candidates must be flexible to work 12-hour shifts when required based on business needs.
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
Duties And Responsibilities
Perform a range of microbiological and biochemical testing, including bioburden, LAL, microbial identification, environmental monitoring (e.g., air, surface, particulate sampling), cell counts, flow cytometry, ELISA, PCR, and compendial testing (pH, conductivity, appearance) in accordance with USP, JP, and EP standards.
Analysis of bulk product according to Standard Operating Procedures and Test Methods.
Documentation of results in accordance with current Good Manufacturing Practices (cGMP).
Problem solving of analytical methods as well as troubleshooting of equipment.
Involvement in method transfers and validation.
Involve in equipment qualification and technical selection of QC equipment and/or standards and reagents.
Generation of required trending and reporting information, document revision and update.
Support / Perform laboratory OOS, deviation investigations.
General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares, autoclaving etc.
Any other duties as assigned by your Supervisor/Manager
Education / Experience
Degree/Diploma in a relevant Science field or Equivalent
2 – 3 years' experience in Quality Control
Strong knowledge of microbiological laboratory operations in a manufacturing environment
Demonstrates an ability and desire to learn from experience
Good problem solving and analytical skills
Good communication skills
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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