About this role
Pharma Quality Specialist Consultant at PA Consulting. Location: Melbourn or London. Role: designing QMS, leading validation, conducting audits Requirements: 8+ years in pharmaceuticals/biotech life sciences with GxP QMS transformation experience, QMS design/implementation, CSV and data integrity, supplier audits, RIM/PLM implementations; QP status desirable. Category: Business Development Seniority: Senior Level Tools: Regulatory Information Management (RIM), Product Lifecycle Management (PLM), computer system validation (CSV) Certifications: qp Commitment: Full Time Workplace: Hybrid Languages: English