About the role
AI summarisedSupport safe, compliant, and efficient manufacturing operations at the Singapore site. This role involves working across manufacturing, quality, maintenance, and technical teams to solve complex problems, drive process improvements, and enable reliable production in a dynamic biopharma environment.
BiopharmaOnsiteManufacturing
Key Responsibilities
- Lead and manage complex deviation investigations and corrective actions to timely closure.
- Design and deliver process improvement projects to increase yield, reduce variability, or raise efficiency.
- Support validation, trials, and technical transfer activities to enable smooth production start-up.
- Monitor process parameters and trends, and support risk assessments for quality and business continuity.
- Prepare clear technical documents, training materials, and work instructions for operations teams.
Requirements
- Bachelor’s degree in Engineering, Biotechnology, Chemical Engineering, Life Sciences, or a related discipline.
- Minimum 4 years of relevant experience in regulated manufacturing (pharmaceutical, biotech, or chemical production).
- Practical experience in deviation investigation and root cause analysis.
- Proven experience with CAPA management.
- Strong troubleshooting skills for process and equipment issues.
- Working knowledge of Current Good Manufacturing Practices (cGMP) and quality systems.