Medical Device UniQuality & Unidata Product Information Specialist

This role is focused on ensuring the accuracy, completeness, and availability of product information related to Medical Devices (MD) within MSF's UniQuality database and MD Repository. The position involves managing entities and quality reviews in UniQuality, updating ISO certificates, enforcing documentation rules in the MD Repository, and coordinating with stakeholders such as International QA MD Coordination teams, European Supply Centres, and field users. Responsibilities include creating, validating, and updating MD entities; ensuring consistency between UniQuality and the MD Repository; training users on Eudamed; proposing improvements to SOPs; and implementing data quality controls. The role supports MSF's mission by enhancing supply chain performance, interoperability, and the quality of care through centralized data stewardship and collaboration with diverse stakeholders.

No explicit educational or experience requirements stated in the provided text; however, familiarity with medical device regulations (e.g., Eudamed, FDA registration, ISO certificates), data management systems, and quality assurance processes is implied. Experience with regulatory documentation, database management, and stakeholder coordination is beneficial. Proficiency in English is required; additional languages are a plus.