Thanks to your work at BioNTech, the development work in production shall be advanced and further developed in accordance with GMP regulations. Your duties in detail:
You will be responsible for the internal and external coordination of development work toward GMP production of RNA preparations and correspondingly also supervise the activities at our partner company EUFETS;
In addition, you will be responsible for the exploration and supervision of external contract manufacturers for the production of relevant preparations (e.g. liposomes, RNA nanoparticle preparations, excipients);
In this context, you will explore new technologies for the production of liposomes and RNA nanoparticle preparations;
Last but not least, you will share responsibility for the development of technologies for GMP-compliant production processes (upscaling) for clinical products to market maturity.
What you have to offer
Completed course of study in natural sciences with a doctorate in chemistry, biology, pharmacy or an analogous field;
Very good knowledge in pharmaceutical technology, production processes for pharmaceutical products to be administered parenterally, or nanoparticle preparations;
Good understanding of technological and physical interrelationships with regard to pharmaceutical preparations;
Knowledge of technologies in connection with drug delivery, gene delivery and/or RNA or DNA-based preparations;
Profound knowledge of the requirements for the work under GMP and in the regulated environment.