Analyst, QC (Product Testing - Shift)

Lonza Group; Singapore; On-site; SGD 60,000 - 85,000; Full time

Benefits offered by this job

Competitive compensation

Medical insurance

Transport to Tuas site

Professional growth

Global exposure

Job summary

Lonza is seeking a QC-Analyst in Singapore to perform timely testing of in-process and final product samples in compliance with SOPs and cGMP. You will support lab operations, sample logistics, and analytical methods such as HPLC, CE, and related physiochemical techniques.

The role includes documentation, troubleshooting, and involvement in method transfers and equipment qualification. We value diverse backgrounds and offer professional growth through cross-functional projects and global

Qualifications

• Degree/Diploma in a relevant Chemistry or Science field or equivalent.
• Relevant lab experience, preferably in biotech or medical field.
• Good understanding of HPLC, Empower software, CE, TOC, Osmolality, protein concentration methods.
• Provide support in equipment maintenance and qualification.
• Understanding spectroscopy and chromatography methods including HPLC and protein concentration.
• Willing to work 12 hours rotating shift.

Responsibilities

• Analyze bulk product, in-process or stability samples per SOPs and test methods.
• Document results in accordance with cGMP.
• Troubleshoot analytical methods and equipment.
• Participate in method transfers and validation.
• Involved in equipment qualification and QC equipment/standards selection.
• Perform assay trend analysis, document revision and updates.
• General lab support: housekeeping, equipment maintenance, inventory, supplies ordering.

Skills

HPLC

Capillary Electrophoresis (CE)

TOC

Osmolality

Protein concentration (A280/SoloVPE)

Education

Degree/Diploma in Chemistry or Sciences

Tools

Empower software

Job description

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), 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.
• 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, accordingly 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/Diploma 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, Empower software, Capillary Electrophoresis (CE), TOC, Osmolality, Protein concentration (A280 or SoloVPE) and other physiochemical methods.
• Provide support in 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.
• Willing to work 12 hours rotating shift

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.

Reference: R80547

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.