1. 8–12 years of experience in medical device / IVD labelling. Proven experience leading large-scale labelling remediation/sustenance/merger projects. 2. Interact with cross functional team spread across geographies to gather technical inputs finalize the inputs, in consent with all stakeholders. 3. Strong knowledge of: ISO 15223 / ISO 20417, EU IVDR/MDR and US FDA labelling requirements, eIFU, UDI, symbol implementation, and multi-language labelling. 4. Manage timelines, resources, risks, and stakeholder expectations. Drive prioritization across high-volume portfolios. 5. High attention to detail with a compliance-driven mindset. Good experience with Redline markup preparation and Labelling verification. 6. Proficiency in labelling/artwork tools (Adobe Illustrator, InDesign, etc.). 7. Experience in automation and digital transformation. Exposure to AI/automation in labelling workflows (preferred). 8. Experience in merger/acquisition integration (labelling harmonization) (preferred). 9...