Stellenausschreibung

Your Role:

Support the registration projects for non-active medical devices in ophthalmology
Analysing requirements from regulations that are relevant for approval, examining and evaluating implementation options with relevant stakeholders and the team
Planning, managing and controlling smaller registration projects; implementing concepts and planned actions and ensuring approval
Participate in international projects for new registrations, registration of product changes or changed requirements triggered by changes in regulations
Participate in development projects and change committees on approval-relevant issues and specify normative and regulatory requirements
Work in an international team of Regulatory Affairs Managers who, together with Branding, Business Management and Logistics, ensure the market availability of our products

Your profile

Your ZEISS Recruiting Team:

Nicole Henzelmann, Norman Funk

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Stellenausschreibung