About the role
AI summarisedPfizer invites eligible candidates to join the Career Progression Program (CCP) for Advanced Biopharmaceuticals Manufacturing Executives/Professionals. This 15-month training program offers a pathway into the Quality Control (QC) Laboratory team, providing comprehensive training for those seeking a career in biopharmaceutical manufacturing.
BiopharmaOnsite
Key Responsibilities
- Perform and review analytical testing (In-Process, Raw Materials, API samples) and results accurately according to test methods, site SOPs, and relevant protocols.
- Adhere strictly to ALCOA principles and Data Integrity (DI) requirements during all testing and documentation.
- Highlight abnormalities detected during testing/review and initiate laboratory investigations as required.
- Assist with troubleshooting laboratory technical problems and support laboratory investigations.
- Author GMP documentation, including SOPs, analytical method transfer protocols, and trend reports.
- Maintain QC processes such as reference standards and retention sample management, conducting investigations for associated deviations.
- Participate in 5S team initiatives and maintain good housekeeping while following all safety procedures.
- Conduct training for colleagues from QC and other departments.
Requirements
- Degree in Science (Chemistry)
- Knowledge of cGMPs and ALCOA principles.
- Ability to work in shifts (IPC team).
- Effective problem-solving skills.
- Demonstrated ability to perform in a team setting.
- Must be a Singapore Citizen or Singapore Permanent Resident.