- Tuas Southwest (Singapore) Singapore
全职 Lead Engineer, MSAT (CGT) 工作, 薪水, Lonza Southwest (Singapore) 公司招聘中 - Ricebowl
工作地点
职位描述
岗位职责
Singapore, Tuas Singapore
Lead Engineer, MSAT (CGT)The actual location of this job is in Singapore.
What You Will Get
What You’ll Do
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.
Reference: R75414
Apply
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R68090
Lead Engineer, MSAT (CGT)The actual location of this job is in Singapore.
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 the MRT location near your home to and from the Tuas site.
- Fully paid medical insurance, and option to enrol family members at partially subsidized premiums.
What You’ll Do
- Lead and support technology transfer of customer manufacturing processes into Lonza Bioscience Singapore.
- Partner cross-functionally with Manufacturing, QA, QC, Validation, Supply Chain, and Project Management to enable successful pilot, clinical, and commercial runs.
- Design and execute scale-down studies and process fit assessments to support tech transfer and scale-up.
- Provide on-floor technical oversight during GMP runs, troubleshooting process deviations and driving investigations.
- Monitor process performance, ensure run-to-run consistency, and implement continuous improvements.
- Author and review process documents, protocols, reports, and change controls.
- Support regulatory inspections, audits, and plant start-up activities.
- Strong expertise in cell & gene therapy, GMP/ATMP, and aseptic manufacturing.
- Hands-on experience in adherent human cell culture.
- Experience in deviation management, change control, CAPA (TrackWise preferred).
- Solid data analysis skills (Excel/statistical tools).
- Knowledge of Lean/Six Sigma and structured problem-solving tools.
- A proactive, solutions-oriented communicator who thrives in fast-paced, cross-functional environments
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.
Reference: R75414
Apply
Similar Jobs
R68090
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