Location: Tuas, Singapore

Be part of Lonza’s Quality Control team, where you will play a critical role in ensuring the quality, safety, and compliance of products manufactured for patients worldwide. As a Senior Analyst, QC, you will perform and oversee testing activities, support method transfers and validations, lead laboratory investigations, and serve as a subject matter expert for analytical methods. This role also contributes to continuous improvement initiatives, data integrity compliance, and the development of laboratory capabilities within a GMP-regulated environment.

What you will get

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Opportunities to collaborate with global cross-functional teams.
• Ongoing learning and professional development opportunities.
• Our full list of global benefits can be found here: Lonza Benefits.

What you will do

• Perform and review testing of raw materials, in-process samples, environmental monitoring samples, and finished products in accordance with approved test methods, SOPs, and cGMP requirements.
• Support method transfers, method validations, equipment qualification activities, and troubleshooting to ensure laboratory readiness and compliance.
• Lead Out-of-Specification (OOS), deviation, and laboratory investigations, including root cause analysis, impact assessments, and technical report writing.
• Author and maintain laboratory documentation including Change Controls, test methods, SOPs, protocols, and technical reports.
• Serve as a trainer and technical resource for analytical methods, laboratory practices, and compliance requirements within the QC team.
• Support laboratory operations including reagent and standard preparation, sample management, equipment maintenance, inventory control, and laboratory housekeeping activities.
• Drive continuous improvement, operational excellence, and data integrity initiatives to strengthen laboratory performance, compliance, and efficiency.

What we are looking for

• Degree or Diploma in a relevant Science discipline such as Chemistry, Biochemistry, Biotechnology, Microbiology, Pharmaceutical Sciences, Life Sciences, or equivalent.
• Quality Control experience within a GMP-regulated pharmaceutical, biotechnology, cell therapy, or life sciences environment.
• Hands-on experience in one or more areas including Product Testing, Raw Material Testing, Microbiology/Environmental Monitoring, or Cell Therapy Quality Control.
• Experience with analytical techniques such as HPLC, ELISA, PCR, CE, SDS-PAGE, IEF/icIEF, spectroscopy, TOC, osmolality, flow cytometry, environmental monitoring, or compendial testing.
• Strong knowledge of cGMP requirements, laboratory investigations, data integrity principles, and quality systems.
• Experience supporting method validation, method transfer, equipment qualification, and technical documentation activities.
• Strong analytical, problem-solving, communication, and stakeholder management skills with the ability to work independently in a fast-paced GMP 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.