Global Quality Compliance Lead

Key Responsibilities Coordinate and lead GPO, GVO, and GBO Quality Councils; manage agendas, executive analyses, and action tracking. Identify cross-functional themes and systemic quality issues; elevate appropriately. Partner with QMS Topic Leads and site/OpU leaders to assess risk signals, recurring failure modes, and escalation paths. Evaluate red metric trends, commitment-date performance, and recurring issues; influence senior leaders on priorities, resourcing, timelines, and corrective actions. Provide oversight of QMS documents and site feedback for QMSC review; align OpU leads to QMS topics. Track progress against annual Operating Unit Quality Plans; monitor performance, slippage, dependencies, and resources. Lead quality improvement activities from governance, trend analysis, audits/inspections, and leadership reviews. Lead/support global critical compliance projects with broad OpU impact. Qualifications Required: Bachelor’s in Life Sciences, Pharmacy, Chemistry, Engineering, Quality, or related. 10+ years in quality/compliance/quality systems/regulated manufacturing. Strong QMS governance, risk management, escalation, and quality execution knowledge; strategic analysis and executive communication. Preferred: Experience with quality councils/governance forums. CAPA/metric trending/quality plan management/inspection readiness experience; regulated industry experience (e.g., pharma/biotech); global QMS framework knowledge. Required/Preferred Skills (as listed) Action item management, compliance activities, data integrity, quality risk management, GMP compliance, QMS, quality metrics, process standardization, progress monitoring, driving continuous improvement. Benefits Eligible for annual bonus and long-term incentive (if applicable). Comprehensive benefits include medical/dental/vision, 401(k), paid holidays, vacation, and sick/compassionate days. #J-18808-Ljbffr Scorpion Therapeutics