Quality Director - Cytiva Duncan
Core
Lead Quality Management Representative for a biopharma manufacturing site, ensuring regulatory compliance and optimizing quality systems.
Role type
Senior IC Quality Director
Builds
Compliant biopharma manufacturing operations and quality management systems
Domain
Life Sciences / Biotechnology / cGMP Manufacturing
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Quality Management System (QMS) implementation, Regulatory compliance (FDA/cGMP/ISO), Lean Manufacturing, Six Sigma, Root Cause Analysis, Team leadership, Budget management
Preferred skills
Change management, Strategic partnership, Succession planning
Technologies
QMS IT systems, Statistical analysis tools
Responsibilities
Lead QA/QC functions and ensure regulatory compliance, Implement and optimize the QMS, Collaborate with leadership to drive customer-centric solutions, Build and mentor a high-performing quality department, Lead site audits and monitor KPIs
Seniority
Senior, hands-on IC
