Project Coordinator in Lifecycle Engineering for Ophthalmic Laser Systems (m/f/x)

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.

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 Coordination of the interdisciplinary lifecycle team

Monitoring, coordination and coordination of the content requirements, time frames, resource use and financial resources of the lifecycle projects

Coordination of Lifecycle Project Priorities in cooperation with Management

Monitoring and support of project managers in action and resource planning

Preparation and planning of approvals and change registrations in cooperation with Regulatory Affairs

Series and range planning of the devices

Independent support of lifecycle projects

Review and release of product documents

Support for internal and external audits

University degree in engineering, physics or a comparable discipline

comprehensive experience in the development of safety-critical medical systems, ideally in the lifecycle management of medical devices

detectable experience in the project management of development projects

Knowledge of relevant standards and regulations for safety-critical medical devices

strong communication skills and enforcement capacity as well as a structured and solution-oriented manner

German and English in word and writing

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