Senior Analyst, (QC)

Lonza Group Ltd.; Singapore; On-site; SGD 55,000 - 90,000; Full time

Benefits offered by this job

Career development

Inclusive workplace

Global benefits programme

Collaboration with global teams

Professional development

Job summary

Lonza Tuas, Singapore is seeking a Laboratory QC professional to perform and review testing of raw materials, in-process samples, environmental monitoring samples, and finished products in compliance with cGMP. You will support method transfers, validations, and equipment qualifications while leading investigations and writing technical reports.

The role also involves creating and maintaining lab documentation, training teammates, and ensuring operational readiness and data integrity across the

Qualifications

• 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 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.

Responsibilities

• 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 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.

Skills

Analytical skills

Problem-solving

Communication

Stakeholder management

Education

Degree or Diploma in Science

Tools

HPLC

ELISA

PCR

CE

SDS-PAGE

IEF/icIEF

Spectroscopy

TOC

Flow cytometry

Environmental monitoring

Compendial testing

Job description

Location: Tuas, Singapore

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?