Lead Specialist, Compliance (Audit Management), QA

lonza· SG02 Lonza Biologics Tuas Pte.Ltd.
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📍 SG - Tuas, SingaporeFull time

About this role

 

The Lead Specialist, Compliance (Audit Management) will support Audit activities in accordance with approved SOPs / Policies for a multi-product, cGxP contract manufacturing facility

Find out more about what a life at Lonza in Singapore could look like for you by watching this short video.

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’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’ll do

  • Develop skills as an internal GxP auditor, as required

  • Provide support in backroom / front room in regulatory inspections and customer audits as required

  • Lead in audit walk down preparation and provide feedback as required

  • Lead in audit / inspection response as required.

  • Lead in complex deviation investigations as required.

  • Owns documents of the assigned Quality Process when applicable

  • Develop skills to be Qualified Trainer in area of expertise

  • Subject Matter Expert in one or more area of expertise

What we’re looking for

  • Bachelor’s degree with relevant experience in Quality Assurance within the biopharmaceutical sector.

  • Proven experience in QA operations in a GMP-regulated biopharma environment.

  • Practical experience collaborating with cross-functional manufacturing teams.

  • Solid understanding of quality management systems and GMP compliance requirements.

  • Familiarity with regulatory guidelines such as FDA, EMA, and ICH.

  • Strong analytical, problem-solving, communication, and organizational abilities.

  • Detail-oriented, structured, and a strong team player with a focus on safety, quality, and meeting timelines

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.

Frequently Asked Questions

Is the salary disclosed for the Lead Specialist, Compliance (Audit Management), QA position at lonza?
The salary for this Lead Specialist, Compliance (Audit Management), QA role at lonza is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Lead Specialist, Compliance (Audit Management), QA position at lonza located?
This Lead Specialist, Compliance (Audit Management), QA role at lonza is based in SG - Tuas, Singapore. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Lead Specialist, Compliance (Audit Management), QA role at lonza full-time or part-time?
This is listed as a Full time position. It is posted as a Lead Specialist, Compliance (Audit Management), QA role in the SG02 Lonza Biologics Tuas Pte.Ltd. department at lonza.
Which team or department does the Lead Specialist, Compliance (Audit Management), QA at lonza belong to?
This Lead Specialist, Compliance (Audit Management), QA position is part of the SG02 Lonza Biologics Tuas Pte.Ltd. department at lonza. See the full job description for more information about the team structure and responsibilities.
How do I apply for the Lead Specialist, Compliance (Audit Management), QA position at lonza?
Click the "Apply Now" button on this page. You will be redirected to lonza's official application portal hosted on workday where you can submit your application directly.
When was the Lead Specialist, Compliance (Audit Management), QA job at lonza posted?
This Lead Specialist, Compliance (Audit Management), QA position at lonza was posted on Aug 20, 2026. Apply as soon as possible — early applications are often reviewed first.
Lead Specialist, Compliance (Audit Management), QA
lonza
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