Senior Biotechnologist, MFG (CGT)

Lonza; Singapore; On-site; Confidential; Full time

Benefits offered by this job

Daily company bus services from MRT to

Fully paid medical insurance with (sub

Shift allowances

Learning and development opportunities

Lonza global benefits access

Job summary

Lonza in Tuas, Singapore, is seeking professionals for cGMP manufacturing with aseptic techniques and strict data integrity. You will complete batch records, monitor processes, and support investigations while coaching junior teammates.

The role includes exposure to electronic systems and a pathway for continuous improvement. The position emphasizes manufacturing excellence, GMP-compliant operations, and a rotating shift environment at Lonza's Tuas site, with opportunities for professional

Qualifications

• Degree or equivalent qualification in Biotechnology, Biochemistry, Life Sciences, or Engineering.
• Hands-on experience in biopharmaceutical manufacturing or GMP-regulated environments.
• Strong knowledge of cGMP, aseptic techniques, cleanroom operations and data integrity requirements.
• Experience in process or equipment troubleshooting, deviation investigations, CAPAs and change controls.

Responsibilities

• Execute cGMP manufacturing activities, ensuring aseptic techniques, cleanroom practices and approved procedures.
• Complete and review Batch Records, logbooks and GMP documentation accurately and on time, maintaining data integrity.
• Perform environmental monitoring, equipment preparation, cleaning and routine production support activities.
• Monitor critical process parameters, troubleshoot equipment and process issues, and escalate non‑routine events.
• Support complex deviation investigations, CAPAs, change controls and work notifications through electronic systems such as DMS, LIMS and TrackWise.
• Coach and mentor junior team members, maintaining training compliance and supporting technical competency development.
• Drive continuous improvement initiatives and take on additional operational responsibilities, including laboratory oversight when assigned.

Skills

Communication

Problem solving

Teamwork

Coaching

Education

Biotech/ bioengineering/ life sciences degree or equivalent

Tools

DMS

LIMS

TrackWise

Job description

Location: Tuas, 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 services from designated MRT locations to and from our Tuas site.
• Fully paid medical insurance, with family coverage available at partially subsidized premiums.
• Shift allowances and ongoing learning and development opportunities.
• Access to Lonza's global benefits: https://www.lonza.com/careers/benefits.

What you will do

• Execute cGMP manufacturing activities, ensuring compliance with aseptic techniques, cleanroom practices and approved procedures.
• Complete and review Batch Records, logbooks and GMP documentation accurately and on time, maintaining data integrity.
• Perform environmental monitoring, equipment preparation, cleaning and routine production support activities.
• Monitor critical process parameters, troubleshoot equipment and process issues, and escal… non‑routine events.
• Support complex deviation investigations, CAPAs, change controls and work notifications through electronic systems such as DMS, LIMS and TrackWise.
• Coach and mentor junior team members, maintaining training compliance and supporting technical competency development.
• Drive continuous improvement initiatives and take on additional operational responsibilities, including laboratory oversight when assigned.

What we are looking for

• Degree or equivalent qualification or experience in Biotechnology, Biochemistry, Life Sciences, Engineering or a related discipline.
• Demonstrated hands‑on experience in biopharmaceutical manufacturing or a comparable GMP‑regulated manufacturing environment.
• Strong technical knowledge of biopharmaceutical processing, aseptic techniques and cleanroom operations.
• Sound understanding of cGMP, critical process parameters, quality systems and data integrity requirements.
• Experience in process or equipment troubleshooting, deviation investigations, CAPAs and change controls.
• Strong communication, problem‑solving and teamwork skills, with the ability to coach and guide colleagues.
• Ability to work in a cleanroom manufacturing environment and perform a rotating 12‑hour shift pattern.

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.