Labelling Systems Specialist (12-Month Contract)
Core
Develop, maintain, and manage labelling content for medical devices, translating regulatory and engineering requirements into compliant documentation while optimizing processes for an Enterprise Labelling System.
Role type
Labelling Systems Specialist (Regulatory/Technical Writing)
Builds
Compliant medical device labelling content and optimized content management processes
Domain
Medical Devices / Regulatory Compliance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Technical writing, regulatory compliance knowledge, systems thinking, content structuring, cross-functional collaboration, process optimization
Preferred skills
Medical device industry experience, design controls knowledge, document management systems, AI/automation exposure
Technologies
Enterprise Labelling System (ELS), document management systems, structured content platforms
Responsibilities
Develop and maintain labelling content across legacy and enterprise systems; Translate regulatory and engineering requirements into compliant documentation; Contribute to content governance within the Enterprise Labelling System; Ensure accuracy and traceability of labelling artefacts; Collaborate with Regulatory, Quality, Systems Engineering, and Product teams; Support continuous improvement initiatives including digital/AI-enabled solutions
Seniority
Mid-level, hands-on specialist
