Responsibilities And Duties
Proactively drive development of nanoparticle formulations formRNA pharmaceuticals.
Design study plans to optimize formulations for given RNA constructs and therapeutic intervention.
Develop nanoparticle manufacturing technologies for in-house application and transfer to external (GMP) facilities.
Closely interact with other teams, e.g., RNA synthesis, biology, analytics, inside the NeoVac.
Prepare documents and reports to management and to internal and external partners.
Assure high quality standards of experimental research and development work in the laboratory.
Please send CV to ella@neovac.co.uk
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