ZEISS | Germany | 73xxx Oberkochen (Baden-Württemberg) | Permanent position | Full time | Published since: 07.01.2026 on stepstone.de
Regulatory Affairs Manager (m/f/d)
Trust something new, grow beyond itself and redefine the boundaries of the feasible. That is exactly what our employees can and should live daily. To make a sign with our innovations and to enable great. Because there are a lot of fascinating people behind every successful company. In an open and modern environment with numerous development and further training opportunities, ZEISS employees work in a culture characterised by expert knowledge and team spirit. All this is supported by the special ownership structure and the long-term goal of the Carl-Zeiss Foundation: to advance science and society together. Today dare. Inspire tomorrow. Diversity is part of ZEISS. We look forward to your application regardless of gender, nationality, ethnic and social origin, religion, world view, disability, age as well as sexual orientation and identity. Apply in less than 10 minutes. .
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Your tasks • Your profile • What we offer
Seeing beyond - future of medical technology
For more than 100 years, the medical technology of ZEISS has been driving progress in ophthalmology and microsurgery. In ophthalmology, our solutions help to maintain and improve the vision of people at any time of life. In microsurgery, our solutions enable targeted interventions on the diseased tissue, so that small and sensitive organs continue to function optimally ZEISS's medical technology supports medical professionals to improve the lives of patients worldwide. The fact that we have a direct influence on the well-being of our people is our daily drive. Your duties You define and implement regulatory, international approval strategies for complex, demanding development projects with the focus on innovative microsurgical applications in the field of intra-operative visualization and digital imaging in neurosurgery
You work on projects for authorisations or changes in legislation (e.g. EU MDR) with
You create submission dossiers for the global admission of medical devices and monitor the admission status and follow and report
You enter as contact persons for internal areas (R&D, project management, product management, marketing communications, clinical affairs, international RA contact persons in the respective markets) and externally for partners and authorities
You optimize global, multi-site Regulatory Affairs processes and drive them forward
You check and approve product-specific marketing materials
You continuously work in project teams for product new and new developments from product definition to market launch
You have successfully completed university education in a technical, economic, business or comparable course of study
You have several years of experience in Regulatory Affairs in medical technology or comparable professional experience
You distinguish in particular your analytical skills and creativity as well as communication strength and organizational talent in an international environment
You have project management experience and knowledge of economic relationships
You have excellent knowledge of English and German in word and writing; further language skills are advantageous
You have very good user knowledge in MS Office and common software tools
Location
 | ZEISS | |
| 73447 Oberkochen (Baden-Württemberg) | ||
| Germany |
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