About this role
Quality / Document Specialist at Pharmatech, Inc.. Location: Lindon, Utah, United States. Role: maintaining qms, leading investigations, supporting audits Requirements: Maintain and improve QMS, generate/review/approve compliance documents; experience in quality in FDA-regulated/co-manufacturing preferred; strong technical writing, problem-solving, cGMP/GDP knowledge. Category: Quality Assurance Seniority: Mid Level Commitment: Full Time Workplace: Onsite Languages: English