4 May 2017
I joined the Malaghan Institute at the beginning of this year and I will lead the design and validation of one of our GMP (Good Manufacturing Practice) laboratories to bring a new cellular therapy, called CAR-T Cell to production. I will also be responsible for adapting the CAR-T cell manufacturing protocol to Western regulatory standards.
Overall I have 7 years’ experience working on similar projects in United Kingdom and in the United States.
The biggest challenge with setting up this project is to adapt the manufacturing protocol for a new cellular therapy as it was developed overseas to different regulatory standards.