About this role
Director, Quality Systems & Regulatory Affairs at Cefaly. Location: Darien Downtown, Connecticut, United States. Role: managing eQMS, leading audits, conducting submissions Requirements: Bachelor's in relevant field required, 8+ years QA/RA medical device experience, eQMS ownership (Greenlight Guru preferred), audit and regulatory submission leadership, strong documentation and project management skills. Category: Research and Development (R&D) Seniority: Senior Level Tools: Greenlight Guru Certifications: rac, cqe, cqa, asq Commitment: Full Time Workplace: Hybrid Languages: English