Regulatory Affairs Specialist
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Skilled professional with background of computer engineering and deep knowledge of medical devices in health care. Skilled in Publication of Technical documents that is Labelling and Collateral documents.Working experience on EU MDR. Review and approval of documents. Creating database and maintenance of the same. Knowledge on SQL. ISO 13485 Certified, ISO 9001:2015. Knowledge on SAP, Power BI. Great customer facing and service experience.