About the role
AI summarisedThis 15-month structured on-the-job training programme is part of the Career Conversion Programme (CCP) designed to build the next generation of skilled manpower for Singapore’s Biopharmaceuticals manufacturing industry. The role provides critical process and technical support to Manufacturing Operations, ensuring optimal and compliant operation of the Value Stream.
BiopharmaOnsiteManufacturing
Key Responsibilities
- Manage deviation investigations and CAPAs of high complexity related to process or technical events.
- Support Manufacturing Operations in tracking critical process parameters and quality/business-continuity risks.
- Serve as a key participant in the Quality Review Board, explaining trends and supporting compliance.
- Identify, manage, and execute improvement initiatives across batch records/SOPs, process optimization, and Operational Excellence (OE).
- Support Manufacturing Operations in executing validation, trials, development, and technical transfer activities.
- Develop relationships across Value Stream and other departments (MSAT, QA, QC, TS) to ensure operational objectives are met.
- Plan and manage deliverables by utilizing resources effectively for assigned tasks and projects.
Requirements
- Degree in Chemical Engineering, Biotechnology, Life Sciences, or other relevant field.
- Knowledge of cGMP and safety (biosafety).
- Familiarity with Biotechnology equipment and processes.
- Proficiency in troubleshooting equipment and processes.
- Knowledge of Lean Six Sigma tools and Project Management principles.
- Effective communication, team building, and organization skills.
- Ability to work independently with strong problem-solving and analytical skills.