Location: Tuas, Singapore
We have an exciting opportunity for a Biotechnologist to join our Manufacturing Central Operations team at Lonza’s Tuas site. Reporting to the Section Lead/Manager, you will support the manufacture of therapeutic proteins under cGMP conditions while developing technical expertise in manufacturing operations, equipment, and quality systems. This role offers hands-on experience with advanced biopharmaceutical manufacturing technologies and provides a strong foundation for career growth within a world-class manufacturing environment.
What you will get
• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.
• Daily company bus from MRT locations across Singapore to and from our Tuas site.
• Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
• Shift allowances and ongoing learning and professional development opportunities.
• Our full list of global benefits can be found here: Lonza Benefits.
What you will do
• Perform manufacturing operations within a cGMP environment, including equipment operation, process monitoring, routine sanitization, sampling, and laboratory tasks in accordance with approved procedures.
• Operate manufacturing equipment and systems, applying aseptic techniques, performing basic troubleshooting, and supporting validation and equipment preparation activities.
• Complete GMP documentation accurately, including Batch Records, logbooks, LIMS transactions, DeltaV operations, Work Notifications, and Quality Tag-outs while maintaining data integrity.
• Develop technical expertise in manufacturing processes, equipment, critical process parameters, and process flow to support consistent manufacturing performance.
• Collaborate with cross-functional teams including MSAT, Engineering, Quality, and Manufacturing to support production, investigations, and continuous improvement initiatives.
• Maintain training compliance and competency across assigned manufacturing operations, equipment, and GMP requirements while continuously developing technical capabilities.
• Contribute to operational excellence by promoting safety, quality, compliance, and adherence to production schedules.
What we are looking for
• Diploma or Degree in Biotechnology, Biochemistry, Chemical Engineering, Biochemical Engineering, Microbiology, Life Sciences, Engineering, or a related discipline.
• Experience in biopharmaceutical, pharmaceutical, biotechnology, manufacturing, or cleanroom operations is preferred.
• Good understanding of cGMP principles, manufacturing documentation, and quality compliance within a regulated environment.
• Familiarity with manufacturing systems such as DeltaV, LIMS, electronic Batch Records, or other manufacturing execution systems is an advantage.
• Strong technical aptitude with the ability to learn manufacturing processes, troubleshoot equipment, and work independently in a production environment.
• Strong communication, interpersonal, and teamwork skills with a proactive approach to continuous learning and operational excellence.
• Willingness to work in a cleanroom environment, perform rotating 12-hour shifts, and undertake manual handling activities in accordance with operational requirements.
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.
Skills Required
- Diploma or Degree in Biotechnology, Biochemistry, Chemical Engineering, Biochemical Engineering, Microbiology, Life Sciences, Engineering, or related discipline
- Good understanding of cGMP principles, manufacturing documentation, and quality compliance in a regulated environment
- Operate manufacturing equipment, apply aseptic techniques, perform sampling, routine sanitization, and basic troubleshooting
- Complete GMP documentation accurately including Batch Records, logbooks, LIMS transactions, DeltaV operations, Work Notifications, and Quality Tag-outs while maintaining data integrity
- Willingness to work in a cleanroom environment, perform rotating 12-hour shifts, and undertake manual handling activities
- Experience in biopharmaceutical, pharmaceutical, biotechnology, manufacturing, or cleanroom operations
- Familiarity with DeltaV, LIMS, electronic Batch Records, or other manufacturing execution systems
- Strong communication, interpersonal, teamwork skills and a proactive approach to continuous learning and operational excellence
What We Do
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.
