Biotechnologist - cGMP Cell & Gene Manufacturing

Lonza

Singapore

On-site

SGD 42,000 - 64,000

Full time

9 hours ago
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Benefits offered by this job

Daily bus service to Tuas site
Fully paid medical insurance with some
Shift allowances
Learning and development opportunities

Job summary

Lonza in Singapore's Tuas site is seeking a hands-on manufacturing associate to contribute to cGMP operations and aseptic processing in a dynamic biopharmaceutical environment.

You will work across batch record review, environmental monitoring and routine production support, using DMS, LIMS and TrackWise to ensure data integrity and compliance. A rotating 12‑hour shift and continuous learning opportunities are offered.

Qualifications

  • Degree or equivalent qualification in Biotechnology, Biochemistry, Life Sciences, Engineering or a related discipline.
  • Knowledge of biopharmaceutical manufacturing, aseptic processing or cleanroom operations is an advantage.
  • Basic understanding of cGMP principles, quality requirements and data integrity practices.
  • Willingness to work in a cleanroom environment and perform rotating 12-hour shifts.

Responsibilities

  • Perform cGMP manufacturing activities in accordance with aseptic techniques, cleanroom practices and approved procedures.
  • Complete and review Batch Records, logbooks and GMP documentation accurately and on time, ensuring data integrity.
  • Perform environmental monitoring and routine production support activities, including equipment cleaning and housekeeping.
  • Operate electronic systems such as DMS, LIMS and TrackWise to support manufacturing and quality activities.
  • Identify and upscale deviations, equipment alarms and other non-routine events in accordance with site procedures.
  • Maintain training compliance and support assigned quality activities, including CAPAs and documentation updates.
  • Participate in continuous improvement initiatives to enhance safety, quality and manufacturing efficiency.

Skills

Strong communication
Teamwork
Shift flexibility
Electronic systems familiarity

Education

Biotech/Life Sciences degree or equivalent

Tools

DMS
LIMS
TrackWise

Job description

Lonza in Singapore's Tuas site is seeking a hands-on manufacturing associate to contribute to cGMP operations and aseptic processing in a dynamic biopharmaceutical environment.

You will work across batch record review, environmental monitoring and routine production support, using DMS, LIMS and TrackWise to ensure data integrity and compliance. A rotating 12‑hour shift and continuous learning opportunities are offered.

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