About the role
AI summarisedThis is a 15-month structured on-the-job training programme designed to build the next generation of skilled manpower for GSK's Biopharmaceuticals manufacturing industry in Singapore. Trainees will be integral members of the Manufacturing Management Team, gaining hands-on experience in a high-performance culture emphasizing quality compliance and continuous improvement.
BiopharmaOnsiteManufacturing
Key Responsibilities
- Supervise, execute, and monitor value stream activities to ensure optimal process operation within cGMP, quality, safety, and environmental guidelines.
- Identify and implement improvements to plant facilities, processes, and operating methods to enhance operational efficiency and minimize risk.
- Lead or support quality/safety investigations using problem-solving tools to determine root causes and implement CAPA.
- Conduct audits and investigations, participating in audit preparations to ensure compliance with GMP and safety requirements.
- Prepare essential manufacturing documents, including LOI, SOPs, and training manuals, adhering to Data Integrity and ALCOA principles.
- Support the Manufacturing Manager during new product introductions or plant trials, completing all necessary documentation on schedule.
Requirements
- Degree in Chemical Engineering
- Must be a Singapore Citizen or Permanent Resident (due to CCP nature)
- Willingness to undergo 15 months of structured on-the-job training
- Commitment to learning and applying cGMP principles in a global supply API manufacturing site setting.