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Manufacturing Quality Manager: Synbionik – Germany

Synbionik is an innovative and expanding biotech start-up that specializes in the production of natural substances through biosynthesis. We are developing a synthetic biology platform from genetically modified microorganisms and suitable bioreactor systems.


  • Transfer of research data into standardized manufacturing instructions for production
  • Creation and maintenance of the pharmaceutical QM system SOPs according to European GMP standards
  • Coordination of applications for manufacturing permits according to §13 I No. 3 AMG
  • Contact for authorities and contract manufacturers in regulatory matters
  • Responsibility for compliance with regulatory requirements as a competent person according to §15 AMG
  • Coordination and management of regulatory affairs service providers


  • License to practice as a pharmacist or master’s degree in a natural science
  • Qualified person according to §15 Medicines Act (AMG)
  • Regulatory knowledge in the context of pharmaceutical production
  • Certification in the field of “Good Manufacturing Practice” (GMP)
  • Knowledge of the Genetic Engineering Act (GenTG) is desirable
  • Very good knowledge of German and English (spoken and written)
  • Structured ability to think and act
  • Ability to work in a team and enjoy working independently


  • Our remuneration is attractive and performance-oriented
  • We are an innovative team and live a collegial atmosphere
  • We offer you a steep learning curve and the opportunity to gain professional experience
  • We warmly welcome new ideas and entrepreneurship
  • We offer flexible working hours
  • We promote your professional development
  • Drinks and fruit are at your disposal
  • Our workplaces are in bright offices and modern laboratories in Frankfurt’s Ostend



Lio Tariman

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