Lohmann & Rauscher GmbH & Co. KG | Germany | 56xxx Neuwied | Temporary contract | Full time | Published since: 12.09.2025 on stepstone.de
Regulatory Affairs Manager Clinical & Biological Evaluation (m/w/d)
A team of over 5,700 employees worldwide. A company with attitude, vision and values of a family business. A modern and forward-looking corporate culture with perspectives. We are looking for top talents who want to introduce and implement know-how, ideas and ambitions in our international teams. L&R is a globally active and expanding company for medical devices. In our core business areas, we develop and produce innovative products and solutions for patients; from high-tech applications in vacuum therapy to modern wound dressing. Take advantage of your chance. We would like to see you in our team Regulatory Affairs Manager Clinical & Biological Evaluation (m/w/d) Quality and Regulatory Affairs | limited to 2 years Your location: Neuwied JOBV1_EN
* After clicking the Read more button, the original advert will open on our partner's website, where you can see the details of this vacancy and contact information. If you need a translation of this text, after returning to our website it will be prepared and you can read it by clicking the Show full translation button.
Your tasks • Your profile • What we offer
A team of over 5,700 employees worldwide. A company with attitude, vision and values of a family business. A modern and forward-looking corporate culture with perspectives. We are looking for top talents who want to introduce and implement know-how, ideas and ambitions in our international teams. L&R is a globally active and expanding company for medical devices. In our core business areas, we develop and produce innovative products and solutions for patients; from high-tech applications in vacuum therapy to modern wound dressing. Take advantage of your chance. We would like to see you in our team Regulatory Affairs Manager Clinical & Biological Evaluation (m/w/d) Quality and Regulatory Affairs | limited to 2 years Your location: Neuwied
Your well-founded know-how is in demand in development projects or in significant product changes: Because you are responsible for the preparation and coordination of clinical and biological evaluations according to the MDR and the ISO 10993 series, as well as the supervision of toxicological opinions – in close coordination with internal specialist departments and external experts. Our specialist departments provide comprehensive and competent advice on subject-specific questions and observe legal requirements for clinical and biological evaluations of medical devices (e.g. MDCG Guidances and ISO 10993 series). You will also support the development of clinical and biological approval strategies and the planning of biocompatibility tests.
Successfully completed study of natural sciences, pharmacy, medicine or medical technology Ideal experience in clinical and biological evaluations of medical devices Very good English in word and writing Self-responsibility and team-oriented working
You want to help shape the future of the medical device industry. We offer you the chance. It is important to keep your profession and private life in balance. We find the right model. Education and training are on your agenda. We encourage you individually in our L&R Academy. JOBV1_EN
Company location
Location
| Lohmann & Rauscher GmbH & Co. KG | |
| Neuwied | ||
| 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.
For more information read the original ad