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Lonza

Senior Analyst, Quality Control (Product Testing)

Posted 2 Months Ago
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In-Office
Singapore
Senior level
In-Office
Singapore
Senior level
Performs biochemistry QC testing for lot release, final products, in-process and stability samples. Maintains GMP documentation and laboratory operations, troubleshoots methods and equipment, supports investigations, qualifications, validation and method transfers, and authors SOPs, test methods and change controls. The role also trains colleagues and ensures testing meets quality, safety and business timelines.
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As a QC-Analyst you will performs timely testing and analysis of in-process and final product samples in compliance with SOPs and cGMP, ensuring accurate documentation and data integrity.
Supports lab operations, sample logistics, and analytical methods (e.g., HPLC, spectroscopy, CE-SDS, icIEF), while contributing to continuous improvement initiatives.


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.


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 will do:

  • To prioritize and perform the various testing/analysis in timely manner, in order to support the business requirements. 
  • Analysis of bulk product, in-process or stability samples, 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. 
  • Involved in equipment qualification and technical selection of QC equipment and/or standards and reagents. 
  • Assay trend analysis, document revision and update. 
  • General lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, management of glass wares etc. 
  • Any other duties as assigned by your Supervisor/Manager

What we are looking for:

  • Degree in a relevant Chemistry, Science field or Equivalent. 
  • Relevant work experience preferably with Lab experience in a biotech or medically related field. 
  • Good understanding of HPLC and Empower software. 
  • Provide support in HPLC equipment maintenance and qualification. 
  • Understanding and execution of spectroscopy, and other assigned methods which may include chromatography methods (HPLC), Protein concentration (A280 or SoloVPE) and other physiochemical methods. 

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.

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