Biotech Operator – Cleanroom Pharma Manufacturing

Lonza

Singapore

On-site

Confidential

Full time

7 days ago
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Benefits offered by this job

Fully paid medical insurance
Shift allowances
Daily bus from MRT to Tuas site
Professional development opportunities
Lifespan of learning and growth

Job summary

Lonza in Tuas, Singapore is seeking a Biotechnologist to join Manufacturing Central Operations - Material & Equipment Preparation (MCO-MEP). You will support the preparation of materials and equipment for cGMP manufacturing of therapeutic proteins in a cleanroom.

You will perform equipment prep, monitor sanitization, KPI‑driven Kanban activities and basic lab measurements while following SOPs and ensuring compliance.

Qualifications

  • NITEC, Diploma or Degree in Biotechnology, Biochemistry, Chemical/Biochemical Engineering or Life Sciences.
  • Related engineering or science disciplines also acceptable.
  • Strong understanding of cGMP concepts is a plus.

Responsibilities

  • Perform material and equipment preparation in a cGMP manufacturing environment.
  • Prepare, monitor and maintain manufacturing equipment and cleanroom areas.
  • Conduct basic lab tasks including sampling, pH, conductivity and osmolality.
  • Document activities in Batch Records, SOPs and LIMS.
  • Develop competency in manufacturing equipment, processes and changeovers (DeltaV).
  • Support deviations, environmental monitoring events, and data integrity reviews.
  • Collaborate with cross-functional teams to troubleshoot issues and maintain schedules.

Skills

Strong communication
Team player
Willingness to learn
Technical aptitude

Education

NITEC/Diploma/Degree in Biotechnology or related

Tools

LIMS
DeltaV

Job description

Lonza in Tuas, Singapore is seeking a Biotechnologist to join Manufacturing Central Operations - Material & Equipment Preparation (MCO-MEP). You will support the preparation of materials and equipment for cGMP manufacturing of therapeutic proteins in a cleanroom.

You will perform equipment prep, monitor sanitization, KPI‑driven Kanban activities and basic lab measurements while following SOPs and ensuring compliance.

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