Job Description
Step out of your comfort zone, excel and redefine the limits of what is possible. That's just what our employees are doing every single day – in order to set the pace through our innovations and enable outstanding achievements. After all, behind every successful company are many great fascinating people.
In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together.
Join us today. Inspire people tomorrow.
Diversity is a part of ZEISS. We look forward to receiving your application regardless of gender, nationality, ethnic and social origin, religion, philosophy of life, disability, age, sexual orientation or identity.
Apply now! It takes less than 10 minutes.
Seeing beyond - future of medical technology
For more than 100 years, ZEISS medical technology has been driving progress in ophthalmology and microsurgery. In ophthalmology, our solutions help to maintain and improve people's vision at every stage of their lives. In microsurgery, our solutions enable targeted interventions on diseased tissue so that small and sensitive organs continue to function optimally. Medical technology from ZEISS supports medical professionals in improving the lives of patients worldwide. The fact that our actions have a direct impact on people's well-being is what drives us every day.
Your Role
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You are significantly involved in the regulatory support of development and change projects.
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You are responsible for the creation and updating of product documentation for medical devices
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Thanks to your knowledge of international product registrations, you play a key role in the international marketability of our medical devices.
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You ensure a smooth process for product registrations and ensure compliance of the products with the requirements of national and international legislation.
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You work closely with interdisciplinary teams (e.g., Global Marketing & Sales, Development, Production, etc.) to ensure a seamless approval of our products.
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You have a completed degree in a relevant field or bring equivalent practical experience.
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Knowledge in the area of regulatory approval and lifecycle management of medical devices according to the MDR and international standards is desirable.
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Practical knowledge in the technical documentation of medical devices is an advantage.
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Familiarity with quality management systems according to ISO 13485 is beneficial.
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Your strong communication skills and problem-solving abilities contribute to you being a valuable team member.
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Fluent English skills; additional language skills are a plus.