Process Engineer | Verfahrensingenieur (m/w/d)

Fraunhofer-Institut für Zelltherapie und Immunologie IZI

Leipzig, Sachsen, Deutschland
Published Feb 23, 2026
Full-time
No information

Job Summary

As a Process Engineer in the 'GMP Biopharmaceuticals' working group at the Fraunhofer Institute for Cell Therapy and Immunology (IZI), you will play a pivotal role in the development of modern biotechnological medicines. Based in Leipzig, your daily responsibilities will center on Upstream Processing (USP), where you will plan and implement sophisticated projects within a Good Manufacturing Practice (GMP) environment. This includes designing new upstream processes, managing material procurement, and providing technical guidance to staff. You will work closely with downstream and filling engineers to ensure seamless workflow integration while maintaining rigorous technical documentation. This position is ideal for professionals who thrive at the intersection of applied research and industrial production. It offers a unique opportunity to contribute to life-saving medical advancements, specifically in cell and gene therapy, within one of the world's leading research organizations. The role balances technical execution with project management and international communication, making it a dynamic career path for those dedicated to healthcare innovation.

Required Skills

Education

Successfully completed university degree in Natural Sciences or Engineering, such as Biotechnology, Pharmaceutical Engineering, Bioprocess Engineering, Biosystems Engineering, or a comparable field of study.

Experience

  • Practical experience working in cleanroom environments up to Class A
  • Professional experience working under GMP conditions
  • Demonstrated experience in the operation of Wave reactors and stirred-tank bioreactors
  • Experience in handling mammalian cell cultures
  • Proven experience in project management and technical documentation within a regulated environment
  • Experience in technical leadership or providing guidance to technical staff

Languages

German (Fluent)English (Fluent)

Additional

  • Expert knowledge of regulatory requirements in the GMP environment, specifically EU-GMP Guidelines Annex I, is required. The role is based in Leipzig and involves working in a highly regulated laboratory environment.