
Medical Device UniQuality & Unidata Product Information Specialist
Category | Grade:ProfessionalDeadline:7 Aug 2026Job ID:2666431Posted on:3 Jul 2026
Overview
Safeguards medical device product information across UniQuality, the Medical Device Repository and UniData. The role maintains data quality, supports product information governance and helps MSF stakeholders use trusted, standardised information for field operations and supply systems.
Department: International Office
Languages
Required: English, French
Job Functions
- Data, Analytics and Artificial Intelligence
- Healthcare and Medical Services
Minimum Experience
5 years
Estimated Salary
Not available
Responsibilities
- Create, validate and update medical device entities in UniQuality according to relevant procedures
- Approve entities for international purchase by checking data completeness in public databases
- Maintain ISO certificate information across UniQuality and the Medical Device Repository
- Ensure regulatory and quality documentation is correctly uploaded, tagged and deduplicated
- Follow Eudamed module updates and train relevant MSF users in practical use of Eudamed
- Propose improvements to procedures and data quality controls for UniQuality and the Medical Device Repository
- Monitor and process product information requests in line with MSF guidelines and standards
- Govern product data so central systems remain accurate, consistent, complete and usable
Requirements
- Master's degree in scientific, engineering, pharmacy or paramedical sciences
- At least 5 years of professional experience in a technical role in scientific, engineering, pharmacy or paramedical sciences
- Detail-oriented, meticulous and organised approach to database entry and modification
- Computer and analytical skills including MS Excel
- Proficiency in spoken and written English
- B2 level of French
Skills
Data StewardshipProduct Information ManagementMedical Device Quality AssuranceRegulatory ComplianceDatabase ManagementData Quality ControlProduct HarmonisationProcess ImprovementUser TrainingStakeholder CoordinationTechnical WritingAnalytical Skills
Tools
UniQualityMD RepositoryEudamedUniDataMS ExcelMDRIVDRISO standardsIATA transport regulations
Additional info
- Contract is 80% and permanent
- Starting date is ASAP
- The successful candidate will by default be contracted through the MSF office in their country of residence at the time of application
- Compensation and benefits follow the package current in the MSF entity establishing the contract
- Reports to the SPINCO Product Information Specialists Coordinator with a functional reporting line to the Deputy Quality Assurance Coordinator for Medical Devices
- Offers are subject to reference checks and appropriate screening checks