At BioNTech, you will make your contribution to the conduct of our clinical studies – because you ensure the development and establishment of GMP-compiant RNA vaccine manufacturing processes. Your duties in detail:
Process development for nanoparticulate mRNA therapeutics for clinical application;
Development and optimization of processes and protocols for GMP-compiant manufacturing of the RNA nanotherapeutics;
Design, planning, preparation, performance, analysis and documentation of experiments in the course of the development projects;
Responsible communication of results and progress reports to internal and external partners;
Method and process transfer to internal and external partners and contract manufacturing organizations.
What you have to offer:
PhD in a science- or engineer-oriented discipline (e.g. chemistry, pharmacy, physics, medicine), best with pharmaceutical technology background, or master's degree plus several years of professional experience or comparable qualification;
Very good knowledge of minimum one of these topics: pharmaceutical technology, colloidal systems as nanoparticles, polymer systems, liposomes, drug/gene delivery
Interest in physicochemical analytics as e.g. light scattering, fluorescence, zeta potential, SAXS;
High standard of spoken and written English. German language skills are advantageous;
High level of organization and reliability. Independent, well-structured and precise way of working. Willingness to take over responsibility, as well as the ability to work in a team and with enthusiasm.