Financial Center Manager - TN North Region

Location: Tuas, Singapore

Be part of Lonza's world-class biologics manufacturing team in Singapore. As a Biotechnologist in our Mammalian Manufacturing operations, you will contribute to the production of life-saving therapeutic proteins while gaining hands-on experience with advanced biotechnology processes in a cGMP environment.

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

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 stations across Singapore to and from the Tuas site.
• Fully paid medical insurance, with the option to enroll family members at partially subsidized premiums.
• Shift allowances.
• The full list of our global benefits can be also found on

What you will do

• Perform cGMP biomanufacturing activities including equipment setup, operation, troubleshooting, and documentation.
• Execute mammalian cell culture and purification processes including bioreactor operations, chromatography, and filtration.
• Monitor process parameters such as pH, dissolved oxygen (DO), CO /O levels, and cell performance.
• Operate and maintain process control systems such as UNICORN and DeltaV while ensuring accurate batch documentation.
• Apply aseptic techniques and maintain cleanroom standards through sanitization and 6S housekeeping practices.
• Prepare buffers, media, and customer-specific solutions while supporting equipment preparation and CIP activities.
• Collaborate with cross-functional teams to ensure safe, compliant, and efficient manufacturing operations.

What we are looking for

• Diploma or Degree in Biotechnology, Life Sciences, Chemical Engineering, or a related discipline.
• Knowledge or exposure to biopharmaceutical manufacturing processes is advantageous.
• Experience working in a manufacturing, laboratory, or cleanroom environment is preferred.
• Familiarity with cGMP practices and regulated manufacturing environments.
• Strong teamwork and communication skills with the ability to work in a collaborative environment.
• Attention to detail and ability to follow standardized procedures and documentation requirements.
• Willingness to work in a rotating 12-hour shift pattern.