BrightOwl Loader Loading

Process Engineer (m/f) Pharmaceutical Production Fill & Finish - Germany  

Company managed [?] Still accepting applications
49 Facebook  Linkedin

Posted on : 10 April 2017

Project Description


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
  • As a part of our lighthouse project , you will soon take the next critical step with us. 
  • With our company, you will become a worldwide forerunner in the development of a completely new type of immunotherapy against cancer using individualized tumor vaccines. 




Your duties in detail:  
  • You will be responsible for setting up and commissioning a filling system for sterile products and for ensuring a smooth filling process in routine production under GMP conditions. 
  • As part of this, you will also be responsible for planning and executing regular qualification and validation tasks. 
  • You will inspect our production documentation, participate in investigating deviations and initiate any necessary action. 
  • In the course of ongoing process optimization in the fill-and-finish area, you will prepare and review SOPs and train our employees. 
  • Once you have displayed your skills in these areas, you will take on additional responsibilities in a leadership role.   




What you have to offer.  
  • A degree in engineering sciences, specializing in bioprocess engineering, pharmacy, chemistry or in a field in the food industry would be an advantage 
  • Several years of solid professional experience in the aseptic filling of pharmaceutical agents under GMP conditions as well as profiency in systematic error analysis. 
  • A further advantage is experience in quality assurance and assessing equipment 
  • Experience in the optimization of production processes and creation of production manuals and standard operating procedures (SOPs) in a GMP environment in both German and English 
  • Highly developed expertise and communication skills required to work with qualification and validation processes as well as to train and manage employees 
  • Willingness to work flexible hours and to accept shift work (including on weekends and holidays)