About the role
AI summarisedManufacturing Engineer at a global biopharma company (GSK) in Singapore. Responsible for designing, improving, and supporting manufacturing processes, leading equipment and facility improvement projects, and ensuring compliance with cGMP and safety standards.
BiopharmaFull-time{'name': 'Engineering'}
Key Responsibilities
- Identify and scope equipment, instrumentation and facility improvement projects to boost safety, quality and productivity.
- Lead front-end design, vendor selection, and project execution across all phases to deliver projects on time and on budget.
- Support commissioning, qualification and validation (IQ/OQ/PQ) activities and prepare test protocols and reports.
- Troubleshoot process and equipment issues, use root cause analysis, and implement robust corrective actions.
- Maintain compliance with current Good Manufacturing Practice (cGMP), health and safety, and data integrity expectations.
- Create and update technical documentation, work instructions and training for operations and engineering teams.
Requirements
- Bachelor's degree in chemical, Mechanical, Biochemical or related engineering field.
- Minimum 2 years' experience in manufacturing or process engineering in pharmaceutical, biotech, or related industry.
- Hands-on experience with process troubleshooting and root cause analysis.
- Experience supporting equipment commissioning, qualification or validation.
- Working knowledge of cGMP and health and safety practices in a regulated manufacturing environment.
- Strong communication and teamwork skills with commitment to respectful collaboration.