About the role
AI summarisedYou will design, improve, and support manufacturing processes at our Singapore site. This role involves close collaboration with operations, quality, engineering, and safety teams to solve complex problems, deliver projects, and drive performance improvements in a dynamic biopharma manufacturing environment.
BiopharmaOnsiteEngineering
Key Responsibilities
- Identify and scope equipment, instrumentation, and facility improvement projects to enhance safety, quality, and productivity.
- Lead front-end design, vendor selection, and project execution through all phases to ensure projects are delivered on time and within budget.
- Troubleshoot process and equipment issues using root cause analysis and implementing robust corrective actions.
- Maintain strict compliance with current Good Manufacturing Practice (cGMP), health and safety standards, and data integrity expectations.
- Create and update technical documentation, work instructions, and training materials for operations and engineering teams.
Requirements
- Bachelor’s degree in Chemical, Mechanical, Biochemical, or a related engineering field.
- Minimum of 2 years’ experience in manufacturing or process engineering within the pharmaceutical, biotech, or a related industry.
- Hands-on experience with process troubleshooting and root cause analysis.
- Proven experience supporting equipment commissioning, qualification, or validation projects.
- Working knowledge of cGMP and health and safety practices in a regulated manufacturing setting.
- Strong commitment to teamwork and excellent communication skills.