About this role
Quality Specialist at VVF. Location: Montgomery, Illinois, United States. Role: Product Release, Audit and Compliance, Documentation and Record Management Requirements: 3-5 years GMP-regulated experience; OTC pharmaceutical manufacturing; product release and audit support; FDA 21 CFR 210/211; USP/ICH; ISO 22716/9001; strong documentation and CAPA skills. Category: Quality Assurance Seniority: Mid Level Tools: TrackWise, MasterControl Commitment: Full Time Workplace: Onsite Languages: English