ISO 13485 Medical Device Quality Management System, Administrative Management
Core
Managing ISO 13485 Medical Device Quality Management System audits, HR operations, and R&D project management for a medical device company.
Role type
Quality Management System Administrator
Builds
Internal audit processes, HR training programs, and R&D project timelines
Domain
Medical Devices / Quality Assurance
Deliverable
dashboards & analysis
Required skills
ISO 13485 audit execution, HR planning, performance evaluation, employee training, R&D project management, regulatory compliance knowledge
Preferred skills
Short-term business travel management, team motivation
Responsibilities
Conducting ISO 13485 system audits, organizing internal and management reviews, liaising with third-party organizations, managing human resource planning and training, overseeing R&D project management
Seniority
Junior, part-time to full-time transition