About the role
AI summarised15-month Attach-and-Train programme for new graduates to become analytical development chemists within GSK’s Singapore biopharmaceutical manufacturing operations. The role focuses on analytical method support, quality compliance, and laboratory investigations under GMP standards.
BiopharmaOnsiteQuality
Key Responsibilities
- Ensure all data supporting the analytical method are accurate and able to take correct actions to address the issue
- Contribute to the plans for the implementation of new testing technologies and methods
- Able to understand and assess the change analytical assessment that may have an impact on product quality, validation and/or current Good Manufacturing Practice (GMP) compliance
- Lead or participate in investigation arising from laboratory investigation, incidents recommendations remedial actions for follow-up
- Draft, review and update appropriate laboratory documents such as testing protocol, procedures, analytical methods and guidelines relating to GMP and operational framework of the laboratory
- Updated with pharmacopeial and other health agencies guidelines
- Ensures that all manufacturing raw materials / non-routine samples and products are analyzed and tested according to the stipulated quality requirements
Requirements
- At least a Degree in Chemistry or relevant science