About this role
Regulatory Affairs & Quality Lead (Region Europe) at Elekta. Location: Stockholm, Stockholm County, Sweden. Role: leading regulatory, ensuring compliance, coordinating submissions Requirements: Experienced regulatory affairs leader in medical devices with strong knowledge of European medical device regulations, quality systems, submission coordination, stakeholder influence, team development, and Microsoft Office. Category: Legal and Compliance Seniority: Senior Level Tools: Microsoft Office Commitment: Full Time Workplace: Hybrid Languages: English