Key Responsibilities include, but are not limited to:
- Lead a team of quality control analysts to ensure the ongoing ability to perform GMP testing of cell and gene therapy materials.
- Set up capability for performing new analytical methods in CGTQC Central Testing Lab, including performing risk assessments, establishing and contributing to the validation of equipment and software and writing / reviewing documentation.
- Ensure change controls, quality deviations, out of specification results, and quality / business risks and actions associated with area of responsibility are appropriately manager and escalated.
- Represent Quality Control during internal audits and regulatory inspections for area of responsibility.
GlaxoSmithKline is a world leading research-based pharmaceutical company that combines both individual talent and technical resources to support our mission to improve the quality of human life by enabling people to do more, feel better and live longer.