About this role
Quality Specialist at Prolaio. Location: Chicago, Illinois, United States. Role: conduct inspections, organize investigations, support monitoring Requirements: Bachelor’s preferred or 2+ years in medical device/pharma production; ISO 13485 and CFR Part 820 experience; regulatory inspections knowledge. Category: Quality Assurance Seniority: Entry Level Tools: ISO 13485, CFR Part 820, Quality Management System (QMS), Environmental monitoring Commitment: Full Time Workplace: Hybrid Languages: English