About the role
AI summarisedThis is a 15-month structured on-the-job training program (Career Conversion Programme - Attach-and-Train) designed to build the next generation of skilled manpower for GSK's Biopharmaceuticals manufacturing industry in Singapore. The role involves becoming an integral part of the Manufacturing Management Team, focusing on changeover operations within a cGMP environment.
BiopharmaOnsiteManufacturing
Key Responsibilities
- Supervise, execute, and monitor changeover activities within the value stream to ensure safe and effective operation compliant with cGMP, quality, safety, and environmental standards.
- Identify and implement improvements to plant facilities and changeover efficiency; troubleshoot decontamination failures and equipment problems to minimize risk.
- Lead or support quality or safety investigations using problem-solving tools to determine root causes and implement Corrective and Preventive Actions (CAPA).
- Conduct audits and investigations, participating in audit preparation and completing assigned actions to ensure compliance with GMP and safety requirements.
- Prepare essential documentation including Local Operating Instructions (LOI), Local Standard Operating Procedures (SOP), and training manuals, adhering to Data Integrity and ALCOA principles.
- Support the Changeover Manager in adopting new technologies and AI tools to enhance changeover efficiency within timelines.
Requirements
- Degree in Chemical Engineering
- Must be a Singapore Citizen or Permanent Resident.
- Commitment to undergoing a 15-month structured on-the-job training program.
- Willingness to work in a high-performance culture emphasizing process automation and quality compliance.