About the role
AI summarisedA 15-month structured on-the-job training programme for entry-level engineers to support biopharmaceutical manufacturing operations at GSK Singapore. The role focuses on process optimization, validation, deviation investigations, and continuous improvement while ensuring cGMP compliance.
BiopharmaOnsiteManufacturing
Key Responsibilities
- Manage deviation investigations and CAPAs of high complexity and related to process or technical events
- Be key participant in the Quality Review Board and be able to explain trends
- Support Manufacturing Operations in tracking process parameters
- Prepare documents and training materials as required to support the activities of the operations department
- Identify, manage and execute improvement initiatives in batch records/SOPs, process optimization, alarms management, and materials management
- Support Manufacturing Operations in executing validation, trials, development and technical transfer activities
- Develop relationship within the Value Stream team and with other departments (including MSAT, QA, QC, TS etc.)
- Plan, manage and execute deliverables through proper and timely request and utilization of resources
- Coach and provide guidance to the Operations Engineer in their execution of daily tasks
- Participate in new technology and/or new process transfer
Requirements
- Degree in Chemical Engineering, Biotechnology, Life Sciences or other relevant field
- Knowledge of cGMP and safety (biosafety)
- Knowledge in Biotechnology equipment and process
- Equipment and process troubleshooting skills
- Knowledge in Lean Six Sigma tools
- Knowledge in Project Management
- Effective communication and team building skills
- Effective organization skills
- Effective project management skills
- Ability to work independently
- Problem solving and analytical skills
- Information search and organization
- MS Office suite of software
- Singapore Citizen or Permanent Resident