Employer profile
Paul-Ehrlich-Institut
Langen, DEImpact-drivenGovernmentHealthcareScience & Research
Impact3Sustainability Goals
Employees201 - 500
About Paul-Ehrlich-Institut
The Paul-Ehrlich-Institut (PEI) serves as Germany's Federal Institute for Vaccines and Biomedicines. Based in Langen near Frankfurt am Main, the organization is responsible for the authorization, evaluation, and safety monitoring of high-risk medicinal products, including vaccines, antibodies, and advanced therapy medicinal products. By combining regulatory functions with internationally competitive research, the institute plays a critical role in safeguarding public health and ensuring the safety of biomedicines.
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Sustainability Goals
Good Health & Well-Being
Ensuring Biomedical Safety and Quality
The Paul-Ehrlich-Institut regulates and monitors vaccines, antibodies, and advanced medicinal products to ensure safe, high-quality medical supplies for the public.
Partnerships for the Goals
Global Health Cooperation
As a World Health Organization collaborating center, the institute engages in extensive international networks to harmonize global standards for vaccine safety and pandemic response.
Industry, Innovation & Infrastructure
Advancing Biomedical Innovation
Through dedicated research groups and fellowship programs, the institute fosters biomedical innovation and supports the next generation of scientists in developing advanced therapeutic approaches.
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FAQs
Q1Where can job seekers find current vacancies at the Paul-Ehrlich-Institut?
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Current career opportunities and vacancies are published on the official federal administration portal at https://karriere.bund.de/die-bundesverwaltung/behoerden-und-organisationen/paul-ehrlich-institut/109.
Q2Where is the Paul-Ehrlich-Institut based?
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The institute is headquartered in Langen, near Frankfurt am Main, Germany.
Q3What is the primary mission of the Paul-Ehrlich-Institut?
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As Germany's Federal Institute for Vaccines and Biomedicines, the organization focuses on the authorization, evaluation, and safety monitoring of high-risk medicinal products, including vaccines, antibodies, and advanced therapy medicinal products.
