Cell Journey Advocate

in Quality Assurance and Logistics. Cycle times will be improved as a direct result of your influence and input.

**Qualifications**:

- 3-7 years CAR-T GMP manufacturing role; or
- 3-7 years CAR-T GxP Technical Operations or manufacturing experience
- An EU Medical Degree with relevant cellular therapy experience is a must-have

Preferred: Knowledge of Oncology/Immunology, cryopreservation of human blood cells, EU Tissue and
- Cell Directives - PhD, Pharm D, Research RN
- 100% fluent in Dutch or French, business proficiency in English
- EU working permit desired; position based in Beerse or Ghent, Belgium
- Available within 12 hours to communicate with FAGG and sites as needed
- Comprehensive knowledge performing tests using and interpreting data from: Automated cell counters, Digital Drop PCR Methods, Multi-color flow cytometry, ELISA methods for cytokines, Cell Culture, BAC-T sterility, Mycoplasma PCR testing
- In-depth comprehension of the implication of any issue to the delivery of a delayed batch
- Self-starter, independent
- Energetic work ethic
- Empathic
- Relatability to all aspects of the cell processing teams
- A minimum of 25% on-site presence