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Accountable for end‑to‑end execution of compliant, accurate, and timely local product labeling and packaging deliverables across assigned MEA markets. Ensures alignment with Global Core Labeling (GCL) and company labeling governance while incorporating local Health Authority requirements, language conventions, and lifecycle changes.
Job Responsibility:
Own and execute local labeling activities for assigned products/country clusters (e.g., SmPC/PI, PIL/leaflet, carton/label text, IFU), ensuring content accuracy, completeness, and compliance
Translate global core updates into local implementation plans: perform impact assessments, draft/redline local texts, coordinate review/approval, and support submission strategy for labeling variations/line extensions
Act as local/regional source text owner for artwork creation: deliver ‘right‑first‑time’ source texts and maintain traceability from CDS/CCDS/GCL changes to country label implementation
Coordinate packaging and artwork lifecycle activities (leaflet, label, blister, outer pack): initiate and manage updates, support shared pack/SKU strategy execution, and ensure supply‑readiness timelines are met
Manage translation workflows (including engaging translation agency systems): request translations, track readiness, and perform 100% translation review for both content and format (as required for regional languages)
Execute labeling/artwork review and approval tasks in designated systems (e.g., Veeva Vault, RIM/Regulatory Information Management, artwork management tools), maintaining version control and inspection‑ready documentation
Monitor and report operational metrics (e.g., right‑first‑time labels, cycle time, on‑time delivery) and drive corrective actions for recurring defects or bottlenecks
Support biosimilars labeling redaction/maintenance activities (as applicable to assigned portfolio)
Support track‑and‑trace/serialization intelligence gathering and execution for assigned clusters
ensure packaging/labeling requirements are reflected in artworks and implementation plans
Draft, update, and/or support local SOPs and work instructions related to labeling management
ensure adherence to internal procedures and quality standards
Identify labeling and packaging risks (compliance, timelines, translations, artwork quality) and proactively propose mitigations
escalate issues per governance
Requirements:
Bachelor’s degree in Pharmacy or related life sciences (required)
advanced degree is an advantage
Typically 4–8+ years of Regulatory Affairs experience with strong hands‑on labeling and artwork/packaging lifecycle management
Current or previous experience within MNCs is a must
Knowledge of Middle East & Africa regulatory requirements and practical experience coordinating multi‑country implementations
Language skills: English (required)
French literacy strongly preferred
Arabic preferred when the role includes Arabic translation review responsibilities
Demonstrated proficiency working in regulated document and workflow systems (e.g., Veeva Vault, RIM tools) and in cross‑functional matrix environments
Skills/behaviors: detail orientation, planning/priority management, proactive risk management, clear written/oral communication, cultural awareness, and a quality mindset
What we offer:
Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits