About this role
Regulatory Affairs & Quality Specialist at Intelerad. Location: Basingstoke or United Kingdom. Role: managing CAPAs, maintaining QMS, conducting audits Requirements: 3+ years in quality management systems, knowledge of ISO 13485/MDSAP/EMDR, IT or medical device experience, MS Office/Google Suite/Visio proficiency, strong communication and problem-solving skills. Category: Quality Assurance Seniority: Mid Level Tools: Microsoft Office, Google Suite, Visio Certifications: raps, rac, asq, cqa Commitment: Full Time Workplace: Remote Languages: English