About this role
Site Quality Associate at Metro Logics, Inc.. Location: Las Vegas, Nevada, United States. Role: audit records, maintain records, train staff Requirements: 5+ years quality/audit experience in cGMP pharma/medical devices; Bachelor's degree or 4+ years supervisory experience; knowledge of cGMP; CQA preferred. Category: Quality Assurance Seniority: Mid Level Tools: GxP, GDP, cGMP, Audit Management Certifications: certified quality auditor (cqa) Commitment: Full Time Workplace: Onsite Languages: English