About this role
Regulatory Expert - Medical Devices at SUSONITY. Location: Carrigtwohill, Ireland. Role: compiling files, supporting compliance, managing submissions Requirements: Bachelor’s or Master’s in life science/engineering,1+ years medical device/IVD regulatory or quality experience,knowledge of MDR/IVDR,FDA 21 CFR 820,ISO 13485,MS Office,strong communication and organization. Category: Legal and Compliance Seniority: Entry Level Tools: Microsoft Word, Microsoft Excel, Microsoft PowerPoint Commitment: Full Time, Contract Workplace: Hybrid Languages: English