CSL Plasma GmbH | Germany | 37xxx Göttingen | Temporary contract | Full time | Published since: 08.04.2026 on stepstone.de
GMP Coordinator (m/f/d)
CSL Plasma is one of the world's largest companies for the production of highly effective coagulation and immunonation products. As a company of the CSL Behring Group, one of the world's largest providers of life-saving biother-apeutics, CSL Plasma is responsible for generating, storing and testing plasma. It is important not only for quality, security and the most modern technology, but above all for our knowledgeable and motivated employees, who contribute to the successful implementation of the objectives set. For our location in Göttingen (Weender Strasse 75 | 37073 Göttingen) we are looking for a
(At the beginning until 30. June 2028 terminated as parental leave)
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Your tasks • Your profile • What we offer
CSL Plasma is one of the world's largest companies for the production of highly effective coagulation and immunonation products. As a company of the CSL Behring Group, one of the world's largest providers of life-saving biother-apeutics, CSL Plasma is responsible for generating, storing and testing plasma. It is important not only for quality, security and the most modern technology, but above all for our knowledgeable and motivated employees, who contribute to the successful implementation of the objectives set. For our location in Göttingen (Weender Strasse 75 | 37073 Göttingen) we are looking for a
(At the beginning until 30. June 2028 terminated as parental leave)
Support team management to ensure GMP compliance. Support for the creation, revision and management of quality agreements including specifications for the production of plasma for fractionation Creation of quality indicators and maintenance of statistics for the department Support of the team in handling electronic quality management systems (eQMS) Support of various existing and implementation of new eQMS in the department and regular user review Creation and processing of internal changes / deviations in eQMS Coordination and tracking of the processing of standard work instructions in the electronic document management system Literature research in the field of EU-GMP guidelines / EU regulations / regulations and laws in the field of plasma extraction and processing
Completed commercial or technical training, 1 – 3 years of professional experience (preferably in health and/or quality assurance) Alternatively: Complete Bachelor's degree in Business Administration or in Natural Sciences, or in Healthcare Very good expression in word and writing in German and English (safe for negotiation) Good knowledge of Microsoft Office package (Excel, Word, PowerPoint, Outlook) Knowledge found in the production of statistics Safe handling of electronic systems First experience in quality assurance desirable Analytical and predictive thinking skills and a pronounced understanding of numbers Impressed communication and motivation Conflictability and Problem Solution Competence Customer and service orientation Teamability and flexibility Independent and structured work Social competence High quality awareness / GxP-friendly work Representative initiative and commitment
We want you to feel comfortable with CSL. That's important and you are. .
Location
![]() | CSL Plasma GmbH | |
| 37073 Göttingen | ||
| Germany |
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