Senior Cell Therapy Manufacturing Lead

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

Benefits offered by this job

Learning & development

Lonza Benefits

Global collaboration

Performance-based rewards

Inclusive culture

Job summary

Lonza in Singapore is seeking a Section Lead to oversee daily operations of a cGMP cell therapy manufacturing team. You will coordinate with QA, Engineering and MSAT to ensure compliant and efficient production, while coaching staff and driving continuous improvement.

The role requires a Life Sciences degree or equivalent and hands-on experience in aseptic processing, cleanroom practices, and proper documentation within a classified manufacturing environment.

Qualifications

• Degree in Life Sciences or equivalent practical experience.
• Experience in cGMP manufacturing with supervisory or team leadership exposure.

Responsibilities

• Lead and develop a high-performing manufacturing team through coaching and performance reviews.
• Plan daily priorities and allocate resources to meet production schedules.
• Oversee production from suite preparation through batch record sign-off with cGMP compliance.
• Ensure timely logbook and first-level batch record reviews; address deviations promptly.
• Guide troubleshooting and issue resolution with QA, Engineering and MSAT involvement.
• Uphold EHS requirements and represent Manufacturing during audits and inspections.
• Drive Operational Excellence and continuous improvement to strengthen cross-team performance.

Skills

cGMP manufacturing

Team leadership

SAP

TrackWise

Quality systems

Communication

Education

Life sciences degree or equivalent

Tools

SAP

TrackWise

Job description

Lonza in Singapore is seeking a Section Lead to oversee daily operations of a cGMP cell therapy manufacturing team. You will coordinate with QA, Engineering and MSAT to ensure compliant and efficient production, while coaching staff and driving continuous improvement.

The role requires a Life Sciences degree or equivalent and hands-on experience in aseptic processing, cleanroom practices, and proper documentation within a classified manufacturing environment.