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. * You develop, maintain, and continuously improve the Quality Management System in accordance with ISO 13485, MDR, and other applicable regulatory requirements - 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 ensure the compliant implementation and application of MED QMS requirements within SAP-supported processes in cooperation with teams * You develop, implement, monitor, and document validation strategies for Computerised System, ensuring compliance with regulatory requierments
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