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Summary: This role focuses on enhancing content quality and improving business processes by transforming regulatory labelling into structured content management to support global affiliates.
Main Responsibilities:
Own and continuously optimize the affiliate content transformation and translation framework.
Define migration methodologies, governance, quality criteria, and best practices in cooperation with the team and stakeholders.
Drive quality assurance of migrated and translated structured content prior to affiliate acceptance.
Collaborate with affiliates to prepare content for migration and identify improvement opportunities.
Monitor migration progress, risks, and bottlenecks; implement corrective actions with team and vendors.
Review migration outputs ensuring traceability, documentation and audit readiness.
Maintain the catalogue of acceptable differences and migration rules.
Support training, coaching, and knowledge sharing across affiliates and project teams.
Key Requirements:
Relevant experience in life sciences, Regulatory Affairs, or documentation management.
GxP and quality management experience.
Experience with documentation or content management.
Process optimization and continuous improvement mindset.
Strong analytical, communication, and planning skills.
Nice to Have:
Experience coordinating cross-functional stakeholders.
Knowledge of Regulatory Affairs or pharmaceutical labelling.
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