Mitarbeiter für Qualitätsdokumentation in Teilzeit (m/w/d)
Core
Creating, updating, and maintaining Standard Operating Procedures (SOPs) and quality documents, coordinating approval processes, and managing metadata in a quality management system.
Role type
Quality Documentation Specialist
Builds
Quality documentation, SOPs, and training materials for pharmaceutical operations
Domain
Pharmaceutical industry, Quality Management
Required skills
Document management, Quality management, Regulatory requirements knowledge, GMP knowledge, Vault Quality Docs administration, LMS administration
Preferred skills
None stated
Technologies
Vault Quality Docs, Learning Management Systems
Responsibilities
Creating and maintaining SOPs and quality documents, Coordinating approval and authorization processes, Managing metadata in the quality management system, Documenting relevant processes and creating reports, Organizing and archiving training materials
Seniority
Mid-level, individual contributor
