RA Professional ERMC Artwork Management
Core
Manage artwork for new labeling and labeling changes to support regulatory submissions and production within the EMEA region.
Role type
Regulatory Affairs Professional (Artwork Management)
Builds
Regulatory submissions and compliant packaging materials for Life Cycle Management processes.
Domain
Healthcare / MedTech / Regulatory Affairs
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Artwork management system usage, regulatory submission coordination, data entry and metrics tracking, quality check (QC) of product information, stakeholder liaison, deadline management
Preferred skills
Virtual team collaboration, independent decision-making, cultural sensitivity, multi-language knowledge
Technologies
Artwork management systems, MS Office, Excel
Responsibilities
Initiate artwork for new labeling or changes to current labeling into production, review artwork and coordinate final approval with Local Operating Companies, monitor metrics for packaging material implementation, liaise with internal and external stakeholders to meet Health Authority timelines, perform or coordinate Quality Check (QC) of local Product Information
Seniority
Mid-level, independent contributor
