Quality Control & Documentation Specialist (Hybrid)

A leading research organization seeks a Project Quality Specialist to support medical device product development teams. Responsibilities include managing documentation according to quality standards, performing document reviews, and ensuring compliance with an ISO 13485 Quality Management System. Candidates should have an Associate's degree and experience in document control or quality assurance, with strong organizational and communication skills. This position offers a flexible work environment with comprehensive benefits. #J-18808-Ljbffr