About this role
Regulatory Affairs Specialist at Sotera Health. Location: Oak Brook, Illinois, United States. Role: maintaining registrations, managing listings, supporting compliance Requirements: Bachelors in life sciences/engineering, 2 years regulatory affairs experience in medical device/pharma/tissue/food, working knowledge of FDA and ISO 13485, familiarity with FDA listing systems, attention to detail; PCQI/FDQI preferred. Category: Legal and Compliance Seniority: Entry Level Tools: FURLS, CDERDirect Certifications: pcqi, fdqi Commitment: Full Time Workplace: Onsite Languages: English