QA Auditor

Lonza; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading life sciences company in Singapore is seeking a Quality Assurance professional to ensure compliance in manufacturing processes. Responsibilities include reviewing documents, overseeing product status, and participating in quality investigations. The ideal candidate holds a degree in Science or Engineering and has experience in cGMP environments. This role offers an agile career and inclusive workplace.

Benefits

Agile career and dynamic working culture

Fully paid medical insurance

Daily company bus to site

Qualifications

• Experience in cGMP manufacturing environment, ideally in Cell and Gene Therapy.
• Hands-on experience with batch record review.
• Proven ability to lead investigations and change controls.

Responsibilities

• Review executed batch records and documentation for compliance.
• Compile lot genealogy and disposition packages.
• Provide QA oversight for product status and shipping documents.
• Support and approve deviation investigations.

Skills

Experience in Quality Assurance

Knowledge of cGMP

Communication skills

Stakeholder management

Batch record review

Deviation management

CAPA implementation

Education

Degree or Diploma in Science or Engineering

Job description

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

What you’ll get

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Daily company bus from the MRT location near your home to and from the Tuas site.
• Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
• Access to Lonza’s full global benefits portfolio: https://www.lonza.com/careers/benefits

What you’ll do

• Review executed batch records, logbooks, and documentation to ensure compliance with cGMP and GDocP.
• Compile lot genealogy and disposition packages to drive timely product release.
• Provide QA oversight for product status, shipping documents, and quality tag‑out systems.
• Support and approve deviation investigations, CAPA implementation, and timely closure of quality events.
• Oversee and approve changes to operational documents (e.g., MBRs, SOPs, Forms, Logbooks).
• Participate in QA shopfloor activities, changeovers, walkdowns, and audits (regulatory/customer).
• Lead and coordinate site projects, investigations, and change controls as needed.

What we’re looking for

• Degree or Diploma in Science or Engineering.
• Experience in Quality Assurance within a cGMP manufacturing environment, ideally in Cell and Gene Therapy (CGT) or biopharmaceuticals.
• Strong knowledge of cGMP, GDocP, and applicable regulatory requirements.
• Hands‑on experience with batch record review, deviation management, and CAPA implementation.
• Proven ability to lead investigations, change controls, and cross‑functional projects.
• Effective communication and stakeholder management skills.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.