about 1 year ago
*Maintaining a GMP manufacturing facility meeting all FDA, EU, MHRA guidelines
*Working with manufacturing teams within a clean room environment
*Be responsible for the technical resource for the manufacturing process
*Compliant to the Quality Management system
*Analyse and write manufacturing reports and review records
* Interactions with Facility management regarding manufacturing activities and warehousing of raw materials
*Ph.D. in Biological sciences and minimum 3 years in a cell therapy field in GMP manufacturing
*T-Cell Manufacturing experience or experience in immunology
*Knowledge of GMP, conforming with EU, FDA and MHRA standards.
*Excellent organisational and communication skills.