About this role
Global Regulatory Specialist at Tobii Dynavox. Location: Stockholm, Stockholm, Sweden. Role: Streamline regulatory, Coordinate audits, Maintain documentation Requirements: Bachelor's in Regulatory Affairs, Life Sciences, Electrical-Electronics or related; 5+ years medical device regulatory affairs with EU MDR and FDA QSR; experience with regulatory systems, audits, and technical documentation; fluent in English. Category: Legal and Compliance Seniority: Mid Level Tools: Regulatory Information Management System, QMS, EU MDR, FDA QSR Commitment: Full Time Workplace: Hybrid Languages: English