About the role
AI summarisedThis is an entry-level Manufacturing Engineer role at GSK's Jurong site in Singapore, part of the Singapore-Industry Scholarship (SgIS) program. The role involves supervising manufacturing operations, ensuring cGMP compliance, driving continuous improvement, and supporting new product introductions in a pharmaceutical API manufacturing environment.
BiopharmaFull-time{'name': 'Manufacturing'}
Key Responsibilities
- To 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 environmental 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, Work Instructions (WI), 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 with 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
- Undergraduate studying a Bachelor's Degree from an accredited university, preferably in Chemical Engineering
- Must be graduated by July 2027 / July 2028 upon joining the programme
- Written and spoken fluency in English
- On-the-job learning with high level of independence in project activities
- Strong written and oral communications skills
- Excellent English proficiency
- Strong analytical and problem solving skills
- A keen interest in production
- Meticulous, organized, and dedicated
- Apply his/her knowledge of communications skills and learn engaging different stake holders to deliver a project
- Effective team player, customer focus, self-driven and the ability to create business solutions
- Good knowledge of cGMP and facility validation for the pharmaceutical industry will be an advantage