About the role
AI summarisedA 15-month attach-and-train programme for Singapore Citizens/PRs to become a Manufacturing Engineer (Changeover) at GSK’s biopharmaceutical plant. The role focuses on supervising and improving changeover activities under cGMP, driving continuous improvement, and ensuring safety and quality compliance.
BiopharmaOnsiteManufacturing
Key Responsibilities
- Supervise, execute and monitor the changeover activities within the value stream to ensure safe and effective operation to achieve efficient changeover process within the framework of current Good Manufacturing Practice (cGMP), quality, safety, occupational hygiene and environment protection
- Identify and implement improvement to plant facilities, and changeover efficiency, troubleshoot for decontamination failures 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 changeover activities, 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.
- Documentation should comply to Data Integrity requirements and adherence to ALCOA principles
- Support the Changeover Manager in adopting new technologies and AI tools to improve the changeover efficiency within the stipulated timeline
Requirements
- Degree in Chemical Engineering
- Singapore Citizen or Permanent Resident