- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 2 weeks ago
- Work mode
- In office
- Education
- Diploma or degree in Biotechnology or related field
- Resume
- Required to apply
Where you'll work
Job description
Company Overview
Join Lonza’s esteemed biologics manufacturing team based in Tuas, Singapore. Contribute to the production of vital therapeutic proteins within a current Good Manufacturing Practice (cGMP) environment, gaining practical experience with cutting-edge biotechnology techniques.
What You Can Expect
- An agile and vibrant career setting with a dynamic corporate culture.
- An ethical and inclusive work environment valuing diversity.
- Compensation plans rewarding outstanding performance.
- Convenient daily shuttle services connecting major MRT stations in Singapore to the Tuas facility.
- Comprehensive medical insurance fully covered by the company, with options to add family members at reduced premiums.
- Shift allowance benefits.
- Access to Lonza’s full suite of global employee benefits.
Key Responsibilities
- Carry out cGMP-compliant biomanufacturing tasks, including setup, operation, troubleshooting, and thorough documentation of equipment and processes.
- Manage mammalian cell culture and downstream purification workflows such as bioreactor operation, chromatography, and filtration technologies.
- Continuously monitor critical process parameters like pH, dissolved oxygen, carbon dioxide/oxygen levels, and cell viability.
- Operate and upkeep process control systems like UNICORN and DeltaV ensuring precise batch records.
- Employ aseptic techniques rigorously and maintain cleanroom standards by following sanitization protocols and 6S housekeeping.
- Prepare process buffers, culture media, and custom solutions, supporting equipment readiness and clean-in-place (CIP) procedures.
- Work collaboratively across functions to uphold regulatory compliance, operational safety, and process efficiency.
Required Qualifications and Skills
- Diploma or Bachelor’s degree in Biotechnology, Life Sciences, Chemical Engineering, or a related field.
- Prior knowledge or practical experience in biopharmaceutical manufacturing is an advantage.
- Experience in laboratory, manufacturing, or cleanroom environments preferred.
- Understanding of cGMP regulations and compliance requirements in production settings.
- Strong communication and team collaboration capabilities.
- Meticulous approach to following procedures and documentation standards.
- Willingness to participate in a rotating shift schedule involving 12-hour work periods.
About Lonza
Lonza is a global leader in life sciences manufacturing with over 30 sites worldwide. We commit to collaboration, accountability, excellence, passion, and integrity in everything we do. We foster a diverse and inclusive workplace where all voices are valued to innovate medicines that improve lives globally.
Additional Information
Location: Tuas, Singapore
Shift Pattern: Rotating 12-hour shifts