Cell & Gene Therapy Manufacturing Specialist (cGMP)

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

Benefits offered by this job

Fully paid medical insurance

Shift allowances

Company bus from MRT locations to Tuas

Job summary

Lonza in Tuas, Singapore, is seeking a manufacturing professional to join the Cell & Gene Therapy team. You will perform cGMP manufacturing activities using aseptic and cleanroom practices, complete batch records, logbooks and GMP documentation, and support environmental monitoring and production activities.

The role involves working with electronic systems (DMS, LIMS, TrackWise), reviewing records, and escalating deviations.

Qualifications

• Bachelor-level degree in a life sciences, engineering or related field.
• Biopharmaceutical manufacturing experience is advantageous but not required.
• Knowledge of aseptic techniques or cleanroom operations is beneficial.

Responsibilities

• Perform cGMP manufacturing activities using aseptic and cleanroom practices.
• Complete Batch Records, logbooks and GMP documentation accurately and on time.
• Perform environmental monitoring, equipment cleaning, sanitization and production support activities.
• Use electronic systems including DMS, LIMS and TrackWise.
• Review Batch Records and logbooks to support timely manufacturing operations.
• Identify and upscale deviations, equipment alarms and other non-routine events.
• Maintain training requirements and contribute to safety, quality and continuous improvement initiatives.

Skills

Attention to detail

Team collaboration

Strong communication

Willingness to learn

Education

Bachelor's degree in Biotechnology/Biochemistry/Life Sciences/Engineering

Tools

LIMS

DMS

TrackWise

Job description

Lonza in Tuas, Singapore, is seeking a manufacturing professional to join the Cell & Gene Therapy team. You will perform cGMP manufacturing activities using aseptic and cleanroom practices, complete batch records, logbooks and GMP documentation, and support environmental monitoring and production activities.

The role involves working with electronic systems (DMS, LIMS, TrackWise), reviewing records, and escalating deviations.