Senior QC Analyst/ QC Analyst (Biochem)

Lonza Group Ltd.; Singapore; On-site; SGD 47,000 - 71,000; Full time

Benefits offered by this job

Agile career culture

Inclusive workplace

Compensation programs recognizing high

Collaboration with global teams

Ongoing learning and professional dev

Lonza Benefits

Job summary

Lonza Group Ltd. in Singapore is seeking a QC-Analyst, Biochemistry to perform analytical testing, support method transfers and validations, and troubleshoot laboratory methods in a GMP environment. You will document data and investigate issues to ensure high quality products.

The role emphasizes collaboration with cross-functional teams, ongoing learning, and contribution to continuous improvement within a fully site-based setting ready to support life-changing therapies.

Qualifications

• Degree or higher in Biochemistry, Biotechnology, Life Sciences, Pharmaceutical Sciences, Chemistry or related field.
• 0–5 years of Quality Control or lab experience in biopharma, biotech, or pharma.
• Hands-on experience with ELISA, PCR, SDS-PAGE, IEF potency assays and Biacore.

Responsibilities

• Perform and prioritize testing of final product, in-process, and stability samples per approved methods and cGMP.
• Execute biochemical and analytical methods including ELISA, PCR, SDS-PAGE, IEF potency assays and Biacore.
• Support method transfers, validations, equipment qualification and lab troubleshooting.
• Document, review, and maintain laboratory data and records per GMP and data integrity.
• Investigate OOS, deviations and analytical issues; support root cause analysis and reports.
• Author and maintain quality documentation including Change Controls, SOPs and methods.
• Contribute to continuous improvement, lab operations, equipment maintenance and training.

Skills

Analytical

Troubleshooting

Problem-solving

Communication

Education

Biochemistry or related discipline

Tools

ELISA

PCR

SDS-PAGE

IEF potency

Biacore

Job description

Join Lonza’s Quality Control team and play a critical role in ensuring the quality, safety, and compliance of biopharmaceutical products that improve lives around the world. As a QC-Analyst, Biochemistry, you will perform analytical testing, support method transfers and validations, troubleshoot laboratory methods and equipment, and contribute to continuous improvement initiatives within a GMP-regulated environment. This role offers the opportunity to work with advanced analytical techniques while supporting the manufacture and release of life-changing therapies.

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 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 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 prioritize testing of final product, in-process, and stability samples in accordance with approved test methods, SOPs, and cGMP requirements.
• Execute biochemical and analytical methods including ELISA, PCR, SDS-PAGE, IEF potency assays, Biacore, and other physiochemical techniques.
• Support method transfers, method validations, equipment qualification activities, and laboratory troubleshooting to ensure operational readiness and compliance.
• Document, review, and maintain laboratory data and records in accordance with GMP requirements and data integrity principles.
• Investigate laboratory events including OOS, deviations, and analytical issues, supporting root cause analysis and technical report generation.
• Author and maintain quality documentation including Change Controls, SOPs, test methods, and laboratory procedures.
• Contribute to continuous improvement initiatives, laboratory operations, equipment maintenance, reagent preparation, and technical training activities.

What we are looking for

• Degree, or higher qualification in Biochemistry, Biotechnology, Life Sciences, Pharmaceutical Sciences, Chemistry, or a related discipline.
• 0 - 5 years of Quality Control or laboratory experience within the biopharmaceutical, biotechnology, or pharmaceutical industry.
• Hands‑on experience with biochemical and analytical techniques such as ELISA, PCR, SDS-PAGE, IEF potency assays, and Biacore.
• Experience supporting method transfers, method validations, equipment qualification, and laboratory investigations.
• Good understanding of cGMP requirements, quality management systems, data integrity principles, and global regulatory expectations including FDA, EMA, and ICH guidelines.
• Strong analytical, troubleshooting, problem-solving, and quality decision‑making skills with the ability to work independently and prioritize effectively.
• Strong communication and interpersonal skills with a collaborative mindset and commitment to safety, quality, and operational excellence.

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?

Every day, our teams across the world work together to turn scientific breakthroughs into life-changing medicines that reach up to 100 million patients a year. Lonza is a place where people can make a unique impact, grow their careers and belong.

You will feel at home at Lonza if you:

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast-moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

Why Lonza: We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters. We are the makers of the medicines of tomorrow. Join us. Be you.