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Research Scientist (m/f) - Germany  

Company managed [?] Still accepting applications

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!
  • We have made our goal to revolutionize the treatment of diseases with cell and gene therapy. Join us in this mission.
  •  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 planning, implementing and maintaining laboratory information and management systems. 
  • In addition, you will handle the organization, documentation and evaluation of analytical tests on critical source materials and clinical trial compounds in quality control. 
  • Naturally, you will also be involved in preparing GMP-compliant documentation. 
  • Moreover, you will qualify the required analytical equipment.    



What you have to offer.  
  • Scientific or technical studies in conjunction with the IT field or equivalent training with several years of LIMS and CSV experience 
  • Experience in administrating laboratory information and management systems, ideally with labware LIMS/ELN, LabVantage or similar computer-based laboratory systems 
  • Interest in the quality control of (bio)pharmaceutical products and experience with analytical methods 
  • Practical knowledge of computer-based laboratory equipment and in processing analytical raw data 
  • Understanding of GMP, knowledge in validating computer systems and practical experience with IT networks and SQL databases in a regulated environment are preferable