Analyst, Quality Control

Lonza; Singapore; On-site; Confidential; Full time

Benefits offered by this job

Agile culture

Inclusive workplace

Competitive pay

Growth opportunities

Medical insurance

Transport to site

Employee benefits

Job summary

Lonza in Singapore is seeking a QC-Analyst to perform timely testing and analysis of in-process and final product samples in line with SOPs and cGMP, ensuring accurate documentation and data integrity. You will support lab operations, sample logistics, and analytical methods (HPLC, spectroscopy) while contributing to continuous improvement initiatives.

Join Lonza to advance your career in a global life sciences leader with access to comprehensive benefits and transport from designated MRT

Job description

Singapore, Tuas, Singapore

As a QC-Analyst you will perform 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), while contributing to continuous improvement initiatives.

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

• Prioritize and perform the various testing/analysis in a timely manner to support the business requirements.
• Analyse bulk product, in-process or stability samples, according to Standard Operating Procedures and Test Methods.
• Document results in accordance with current Good Manufacturing Practices (cGMP).
• Problem‑solve analytical methods and troubleshoot equipment.
• Involve in method transfers and validation.
• Contribute to equipment qualification and technical selection of QC equipment and/or standards and reagents.
• Perform assay trend analysis, document revision and update.
• Provide general lab support including housekeeping, equipment maintenance, inventory of supplies, lab supplies ordering, and management of glassware.
• Execute any other duties as assigned by your Supervisor/Manager.

What We Are Looking For

• Degree/Diploma in a relevant Chemistry, Science field or equivalent.
• Relevant work experience, preferably with laboratory 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.

Reference: R77051