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You will be updated with latest job alerts via emailWork close with the head of department and supervising development projects
Preparing scientific reports as well as development plans
Take over QbD principles and responsibility for the implementation of these in our pharmaceutical development projects
Writing GxP relevant SOPs, scientific consultation and advice to principal scientist and other departments
Support departments like Medical Affairs in CMC and Regulatory Affairs
Close cooperation with the head of department and the Chief Scientific Officer
Gender-Hinweis
Aus Gr nden der besseren Lesbarkeit wird auf die gleichzeitige Verwendung der Sprachformen m nnlich, weiblich und divers (m/w/d) verzichtet. S mtliche Personenbezeichnungen gelten gleicherma en f r alle Geschlechter.
Full Time