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Specialist in packaging and documentation (m/f) Manufacturing of Clinical Trial Samples - 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!  Here, you’ll achieve greatness
  •  At our company you will be responsible for providing samples for testing of new cancer treatment vaccines in clinical trials. 



Your duties in detail:  
  • In collaboration with your team colleagues, you will assemble different pharmaceutical kits by packing product vials according to precise manufacturing instructions (fabrication of micro batches, no clean room work). 
  • You will be responsible for requesting source materials, the proper storage of materials and reliable labeling of the test products under GMP conditions. 
  • This includes completing manufacturing protocols, logbooks and accounting lists in GMP-compliant documentation. Moreover, you will diagnose deviations and assist in creating new operating procedures. 
  • Qualifying devices and maintaining equipment will also fall within the scope of your duties. 
  • In addition, you will perform measurements independently and ensure that maintenance and cleaning intervals are adhered to.   



What you have to offer.  
  • You will have completed vocational training, possibly outside the industry 
  • Experience in packaging, packing, storage logistics or inventory management is desirable 
  • Previous experience in a GMP facility within the pharmaceutical industry (or in a related regulated environment such as the cosmetics or food industry) would be an advantage 
  • Proficiency in writing reports in German as well as basic English skills. Good knowledge of MS Word and Excel 
  • Technical understanding and a conscientious and quality-conscious working style