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Lonza Singapore is seeking a Section Lead to manage a cGMP cell therapy manufacturing team in Tuas. You will guide daily operations, ensure aseptic practices, and maintain data integrity while coordinating with QA, Engineering and MSAT to meet production objectives.
The role requires a Life Sciences degree and prior supervisory experience in a regulated manufacturing environment. Strong problem solving and communication skills are essential.
Location: Tuas, Singapore Today, Lonza is a global leader in life sciences. Our greatest scientific solution is talented people working together, devising ideas that help businesses help people. In exchange, we let our people own their careers. Their ideas, big and small, improve the world. And that’s the kind of work we want to be part of. Join our Singapore manufacturing team and contribute to the production of innovative cell therapies. As Section Lead, you will lead the daily operational and administrative activities of a cGMP Cell Therapy manufacturing team, ensuring safe, compliant and efficient production. You will partner with Quality Assurance, Engineering and Manufacturing Science and Technology (MSAT) to resolve issues, strengthen consistency across teams and deliver production objectives.
Lead and develop a high-performing manufacturing team through coaching, on-the-job training, performance reviews and development planning. Plan daily priorities and allocate resources to meet production schedules, ensuring manufacturing suites, equipment, materials and documentation are ready for each shift. Oversee production from suite preparation through batch record sign-off, maintaining consistent aseptic practices, cleanroom behaviour, cGMP compliance and data integrity. Ensure timely logbook and first-level batch record reviews, address review comments and initiate deviations promptly when required. Guide troubleshooting and issue resolution, escalating risks appropriately and coordinating with QA, Engineering and MSAT to support smooth operations. Uphold site Environmental, Health and Safety (EHS) requirements and represent Manufacturing as a subject matter expert during customer audits and regulatory inspections. Drive Operational Excellence and continuous improvement initiatives to strengthen cross-team consistency, process efficiency, product quality and right-first-time performance.
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.
You will feel at home at Lonza if you:
We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, you 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.