GMP Manager Manufacturing

GMP Manager Manufacturing


Mainz, Germany

Here, you’ll achieve greatness

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.

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BioNTech     Germany     Manufacturing and Logistics     Quality Assurance     5 Years+ Experience    

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