Mitarbeiter Qualitätsmanagement - Pharma (m/w/d)
Core
Ensuring quality compliance in a pharmaceutical manufacturing environment through deviation management, CAPA, risk analysis, and GMP documentation.
Role type
Quality Management Specialist (Pharma)
Builds
GMP-compliant processes and documentation for pharmaceutical production
Domain
Pharmaceutical manufacturing / Quality Assurance
Required skills
Deviation management, CAPA handling, Risk analysis, GMP documentation, Audit support, Process optimization
Preferred skills
IT affinity, Independent coordination
Technologies
GMP documentation systems, Audit tools
Responsibilities
Review and process deviation management (AWM) and CAPA processes, Monitor risk analysis (RiAs), Create/edit GMP documents including Contaminations-Control-Strategy, Support internal/external audits and self-inspections, Optimize documentation structures and paper-based GMP processes
Seniority
Mid-level, hands-on specialist
