Regulatory Affairs Administrator
Core
Coordinate regulatory block and release activities for medical device products and spare parts to ensure compliance and timely availability.
Role type
Regulatory Affairs Administrator (Medical Devices)
Builds
Regulatory release workflows and product compliance status for global operations
Domain
Medical Devices / Healthcare
Deliverable
production ML models | product features | dashboards & analysis | client delivery | infrastructure | physical/clinical work
Required skills
ERP systems proficiency, regulatory compliance knowledge, process improvement, data analysis, stakeholder collaboration
Preferred skills
Medical device industry experience, Microsoft Office proficiency, proactive problem solving
Technologies
ERP systems, Microsoft Office (Word, Excel, Outlook, Teams)
Responsibilities
Coordinate regulatory block and release activities, maintain product status in ERP systems, review release forecasts, monitor process performance, update product catalogue content, support compliance initiatives
Seniority
Mid-level, hands-on IC
