Key Duties and responsibilities

1. Production of advanced cell therapy products in accordance with GMP (B-grade)
2. Buffer and medium preparation
3. Small- and large-scale cell cultivation
4. Sampling and analysis of process samples and environmental monitoring samples
5. Reporting deviations and participating in deviation investigations
6. Documents work performed in batch protocols and logbooks
7. Prepares and updates SOPs
8. Evaluate results and data of the process

Equipment responsible

That all work is performed in accordance with GMP, Cellcolabs' QMS, and, when relevant GDP/GCP