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GMP Manager (m/f) Manufacturing Mainz Germany,  

Biontech (company)

Posted on : 10 April 2017

Project Description

  •  Everyone achieves greatness at our company.
  •  As one of the most rapidly growing biotechnology companies in Europe, we re working on revolutionary approaches in the fight against cancer and other diseases. 
  • Over 500 dedicated, passionate pioneers achieve sensational success and promising breakthroughs time and again by forging new paths  and ensure people all around the world have hope for the future. 
  • You too can become a pioneer!  Here, you ll achieve greatness
  • Thanks to your work at our company , 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
  • In addition, you will be responsible for the exploration and supervision of external contract manufacturers for the production of relevant preparations.
  • 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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