Third Party Specialist
Core
Coordinate, document, and monitor third-party suppliers and contractors supporting GxP activities in pharmaceutical manufacturing, distribution, and clinical operations.
Role type
Quality Assurance Third-Party Specialist
Builds
Compliant supply chain and vendor ecosystem for clinical research services
Domain
Life Sciences / Clinical Research / Quality Assurance
Required skills
GxP compliance, vendor qualification, risk assessment, CAPA management, audit coordination, regulatory knowledge (GMP/GDP), supplier performance monitoring
Preferred skills
Pharmaceutical sciences background, cross-functional collaboration, inspection readiness expertise
Technologies
Quality management systems, audit tools
Responsibilities
Manage supplier qualification and requalification, maintain Approved Supplier Lists, coordinate risk assessments and due diligence, monitor supplier performance metrics, support CAPA tracking, assist in internal and external audits, contribute to inspection readiness
Seniority
Mid-level, hands-on IC
