Senior Cell Therapy Manufacturing Lead (cGMP)

Lonza Biologics Tuas Pte Ltd

Singapore

On-site

Confidential

Full time

2 days ago
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Benefits offered by this job

Agile culture
Inclusive workplace
Professional development
Global collaboration

Job summary

Lonza Biologics Tuas Pte Ltd in Singapore is seeking a Section Lead for our cGMP Cell Therapy manufacturing team. You will guide daily operations, ensure compliance, and drive safe, efficient production across shifts.

You will collaborate with QA, Engineering and MSAT to resolve issues, review batch records, and support continuous improvement. Strong leadership and GMP knowledge are essential to maintain data integrity and right-first-time performance.

Qualifications

  • Degree in Life Sciences or equivalent or practical experience.
  • Experience in cGMP manufacturing with supervisory or team leadership exposure.
  • Proficiency with SAP and TrackWise/documentation workflows.
  • Strong communication and cross-functional collaboration skills.
  • Attention to detail and ability to prioritise resources and decisions.

Responsibilities

  • Lead and develop a high-performing manufacturing team through coaching, training, and performance reviews.
  • Plan daily priorities and allocate resources to meet production schedules.
  • Oversee production from suite prep to batch record sign-off with cGMP and data integrity.
  • Ensure logbook and batch record reviews and address deviations promptly.
  • Coordinate with QA, Engineering and MSAT to support smooth operations.
  • Uphold EHS requirements and support customer audits and inspections.
  • Drive Operational Excellence and continuous improvement across teams.

Skills

Leadership
Coaching
Communication
Problem solving
Decision making
Prioritization

Education

Bachelor's in Life Sciences

Tools

SAP
TrackWise

Job description

Lonza Biologics Tuas Pte Ltd in Singapore is seeking a Section Lead for our cGMP Cell Therapy manufacturing team. You will guide daily operations, ensure compliance, and drive safe, efficient production across shifts.

You will collaborate with QA, Engineering and MSAT to resolve issues, review batch records, and support continuous improvement. Strong leadership and GMP knowledge are essential to maintain data integrity and right-first-time performance.

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