Quality Manager Engineering (f/m/x) - limited for 1 year

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 set the pace with our innovations and make it great. Because there are a lot of fascinating people behind every successful company. ZEISS employees work in an open and modern environment with numerous development and further training opportunities. Our culture is characterized 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.

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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.

support and monitor the development process in development projects for innovative medical devices

Take responsibility for product quality and good documentation practice

as Risk Manager (m/w/x) manages the risk management team and together with it identify, evaluate, evaluate and mitigate risks for patients, users and third parties and maintain the risk file throughout the product life cycle

contribute to the design FMEA and ensure the implementation and effectiveness of the measures

ensure the reliability of the product by means of appropriate development methods and tests

check and release the test plan for the series-accompanying test, the initial sample test, and the design verification test plan

Root-Cause analyses initiate the processing of customer complaints and corrective and preventive measures

Advise project leaders and project teams in the effective and efficient application of the processes and support process owners in improving the processes

support in the preparation and implementation of external and internal audits

a master or a diploma in an engineering or scientific field or a comparable qualification

Professional experience in development projects in manufacturing, ideally in a highly regulated environment such as medical technology

pronounced analytical, structured and solution-oriented work

Team skills, organizational skills and a careful and performance-oriented approach

Experience in risk management according to ISO 14971 or comparable standards

Knowledge of reliability management (or reliability / dependability)

Knowledge of fault analysis and technical statistics in quality management

Knowledge of Medical Standards and International Medical Device Law

broad basic knowledge of optics, mechanics, electronics and software

Exercise in dealing with Office programs, ideally also with Minitab, Polarion, SAP and APIS IQ

Experience in cooperation with international development partners and suppliers

knowledge of English and German in word and writing

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