About the role
AI summarised15-month attach-and-train programme for Singapore Citizens/PRs to become Manufacturing Engineers within GSK’s biopharmaceutical value streams. Role involves supervising production, driving continuous improvement, ensuring cGMP compliance, and leading quality/safety investigations while receiving structured on-the-job training.
BiopharmaOnsiteManufacturing
Key Responsibilities
- Supervise, execute and monitor the activities within the value stream to ensure reliable and optimal operation of processes, equipment, utility and facility so as to achieve target production levels within the framework of current Good Manufacturing Practice (cGMP), quality, safety, occupational hygiene and environment protection
- Identify and implement improvement to plant facilities, processes, methods of operations and turnaround, troubleshoot for process and equipment problems to minimize safety and quality risk as well as to ensure greater operational efficiency
- Lead or support quality or safety related investigation using appropriate problem-solving tool to determine the root causes and implement CAPA to prevent recurrence
- Conducts audits and investigations, participate in audit preparation and complete identified actions in the assigned work area(s), in order to ensure compliance with GMP and safety requirements
- Prepare documents relating to manufacturing, plant turnaround, Local Operating Instructions (LOI), Local Standard Operating Procedures (SOP) and training manual to ensure that updated documents exist to support the activities of the operations department, schedule plan orders, and materials assignment.
- Documentation should comply to Data Integrity requirements and adherence to ALCOA principles
- Support the Manufacturing Manager in new product introduction or plant trials and prepare and complete all necessary documents related to plant trial within the stipulated timeline
Requirements
- Degree in Chemical Engineering
- Singapore Citizens and Permanent Residents only