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Posted on : 09 May 2017
Everyone achieves greatness at BioNTech! 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! At EUFETS, it is our aim to revolutionize the treatment of diseases using cell and gene therapy. Join us in this mission in Idar-Oberstein! Here, you ll achieve greatness. At EUFETS, you will be making an important contribution to the development of cell and gene therapy medicinal products, cellular medical products and gene therapeutics for use in clinical studies. Here s a look at your specific responsibilities: You will take over the quality management of the cell and virus production or the production of RNA. In this context, you are responsible for regulatory and QM support of our customers. In addition, you will be responsible for creating, reviewing, and releasing GMP-relevant documents. The batch record review of the manufactured products will take a lot of your daily work. Naturally, you will also help to qualify suppliers and service providers and help to establish new projects. What you have to offer. Degree in biotechnology or similar Experience in the production or quality control of cell and virus products or in vitro transcribed RNAs Good knowledge of GMP regulations and practical experience in the QM field. Good German and English skills as well as MS Office knowledge Have we kindled your pioneering spirit? Then apply now for our location Idar-Oberstein and look forward to becoming part of a highly qualified, motivated, and collegial team, in which you can expect exciting tasks and new career prospects. Simply send us your application documents using our online form. If you have any further questions, please contact Simone Gans +49 (0) 6781 9855-210.
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