As a Senior Regulatory Affairs Specialist, you will work closely with all departments and be mainly responsible to prepare / review and maintain the technical documentation according MDR 2017/745 (EU) and preparation, review and maintenance as well as submissions for international approval. * Responsible for the creation, review and maintenance of technical documentation * Appropriate Science or Engineering Degree, preferably in medical technology, or equivalent combination of education and experience in the field of technical documentation and manufacturer information * development, risk management, project management, Vigilance, PMS, CAPA, Complaints, etc.)
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