Senior RA Specialist/RA Supervisor
Core
Manage day-to-day product registration operations and ensure timely completion of regulatory tasks in compliance with local laws and guidelines.
Role type
Senior Regulatory Affairs Specialist
Builds
Regulatory dossiers, submission documents, and promotional materials
Domain
Pharmaceuticals
Required skills
Product registration management, regulatory dossier compilation, regulatory agency communication, review of promotional materials, technical documentation preparation, regulatory compliance, competitive intelligence collection
Preferred skills
Product registration strategy development, tender application support, pricing submission support, custom clearance support
Technologies
MS Office Applications
Responsibilities
Perform and manage day-to-day product registration operations, compile registration dossiers and prepare regulatory documents, communicate with regulatory agencies, follow up on review processes, maintain regulatory documentation, collect regulatory and competitive information, review promotional materials, support hospital enlisting and tender applications
Seniority
Mid-level, hands-on IC