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Assistance (m/f) - Germany  

Company managed [?] Still accepting applications

Posted on : 09 May 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 implement the tasks within the QM system and ensure the swift availability of documents for audits and inspections. 


Your duties in detail:  
  • You will support the QM-Team with batch record review of drug products for clinical use. 
  • Moreover, you will help the Qualified Person with the batch certification. 
  • In this context, you will also take care of the administration of the retention samples of produced batches. 
  • You are responsible for the GMP archive. 
  • Last but not least, you will also be involved in general QM tasks.   



 What you have to offer.  
  • Successfully completed training as BTA, MTA, biology lab tech certification or related qualification 
  • Understanding of how complex facts are captured, and the ability to formulate them succinctly and intelligibly 
  • Independent, precise, and dependable approach to work 
  • Good German and English skills as well as MS Office knowledge in Word and Excel 
  • Good knowledge about relevant GMP regularities and base knowledge about QM systems and practice experience with the manufacturing and testing of drugs are preferable but not provided