Octapharma Produktionsgesellschaft Deutschland mbH | Germany | 31xxx Springe | Temporary contract | Full time | Published since: 01.04.2026 on stepstone.de
Clerk/Quality Management Expert (m/f/d)
Be part of a vital chain and contribute to our common goal of improving the lives of people. Octapharma is one of the world's largest manufacturers of drugs based on human proteins and develops and produces drugs from human plasma and human cell lines. We are a privately run company where the warmth of a family atmosphere meets the strength of a global organization.
The Octapharma production company Deutschland mbH (OPGD) in Springe near Hannover is one of five state-of-the-art production sites. There we produce with our around 850 employees: a finished product and intermediate products for further processing.
In your role as a specialist/expert (m/w/d) quality management, you are responsible for the GMP-compliant plasma documentation. This position is searched in full time with 38.5 hours per week and at first 24 months. Design our vision to create new health solutions that improve people's lives. .
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Your tasks • Your profile • What we offer
Be part of a vital chain and contribute to our common goal of improving the lives of people. Octapharma is one of the world's largest manufacturers of drugs based on human proteins and develops and produces drugs from human plasma and human cell lines. We are a privately run company where the warmth of a family atmosphere meets the strength of a global organization.
The Octapharma production company Deutschland mbH (OPGD) in Springe near Hannover is one of five state-of-the-art production sites. There we produce with our around 850 employees: a finished product and intermediate products for further processing.
In your role as a specialist/expert (m/w/d) quality management, you are responsible for the GMP-compliant plasma documentation. This position is searched in full time with 38.5 hours per week and at first 24 months. Design our vision to create new health solutions that improve people's lives.
Processing & Testing of the Documentation on Plasma Delivery Investigations and evaluations of the transport temperature of plasma (optional intermediates and final products) Testing and approval of the plasma for production according to regulatory requirements Treatment of plasma donations and their risk assessments Maintenance and management of relevant plasma data in internal computerized systems (ERP/MES) Support in internal and cross-departmental initiatives/projects
Completed commercial or scientific training or comparable Career experience in conscientious documentation / expertise in a global team is desirable Secure IT user knowledge (MS Excel, Word), SAP knowledge of advantage Good knowledge of relevant standards & laws (GMP/Ph. Eur./CFR) Very good knowledge of German and English Careful and targeted operation Teamability and flexibility Your department where you do something The area of quality carries the overall responsibility for the quality control and safety of our medicines with the aim of ensuring the safety of our patients. The Corporate Quality Plasma department ensures the GMP-compliant documentation of human plasma donors according to regulatory requirements.
You help to save lives - every day is important, because we make life-saving drugs Social benefits - employer-funded occupational pensions, long-term account, Hansefit, Benefit portal with advantageous offers, bicycle leasing, external health coaching and regular company celebrations Expertise development – We offer various internal and external employee and executive training, trainee programs and digital solutions Miscellaneous - With us you can start the short Friday earlier in the weekend
Location
![]() | Octapharma Produktionsgesellschaft Deutschland mbH | |
| 31832 Springe | ||
| Germany |
The text of this ad was translated from German into English using an automatic translation system and may contain semantic and lexical errors. Therefore, it should be used for introductory purposes only. For more detailed information, see the original text of the ad at the link below.
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