Supporting the management of global, regional, and local procedural documents, the full-time Global Document Management Manager will oversee the development and improvement of the Quality System, assist with GxP inspections, and manage Standard Operating Procedures while working remotely. Key Responsibilities Support the development, implementation, and continuous improvement of the Quality System across GxP-related functional areas Assist in the preparation for GxP inspections and responses to Regulatory Authorities Manage the development and revision of global Standard Operating Procedures and Working Practices to ensure regulatory compliance Required Qualifications Degree in natural science or equivalent experience 4+ years of relevant experience in clinical, industry, or Regulatory Authority settings, preferably in Quality Management Advanced knowledge of regulations and guidance documents related to Pharmacovigilance, Clinical Development, and Regulatory Affairs Experience in Monitoring, Quality Assurance, and Good Clinical Practices Proficiency in MS Office and understanding of change management processes