Key Duties and responsibilities
- Production of advanced cell therapy products in accordance with GMP (B-grade)
- Buffer and medium preparation
- Small- and large-scale cell cultivation
- Sampling and analysis of process samples and environmental monitoring samples
- Reporting deviations and participating in deviation investigations
- Documents work performed in batch protocols and logbooks
- Prepares and updates SOPs
- 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
Hur du söker jobbet
Ansökan sker via e-post till [email protected].