Based in Texas, Onsite
As a Principal Scientist in Downstream Process Development, you will play a crucial role in this clients project team, contributing to the experimental design, planning, and development of downstream processes for innovative therapeutic products. This position will focus on utilizing adeno-associated viruses and Lentivirus to develop Gene Therapies.
Requirements :
- 3 years + of downstream process development experience with AAV's / LV.
- Experience working within a CDMO environment or small start up.
- SME for downstream AAV and Lentivirus processes, collaborating closely with the upstream Process Development team.
- GMP manufacturing experience.
To hear more about this exciting, innovative opportunity please give me a call on 857 4007901 or email me shannon@greenlsr.com
