You plan, drive, and document risk management activities across processes and projects As Quality Management System (QMS) Manager (m/f/x) you are responsible for establishing, maintaining, and continuously developing an effective Quality Management System in compliance with applicable medical device regulations. The focus of the role is the coverage of Computerised System Validation (CSV) and the correct consideration of regulatrory requirements within the implementation phase of ZEISS FIT4 SAP S/4Hana Project. * You develop, maintain, and continuously improve the Quality Management System in accordance with ISO 13485, MDR, and other applicable regulatory requirements * You bring extensive years of professional experience in Quality Management within the medical device, pharmaceutical, or similarly regulated industry
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