Integrated project planning and scheduling using Smartsheet, Microsoft Project, or equivalent Advanced Excel and structured data management, including lookups, pivot tables, reconciliation, filtering, and data validation RAID and dependency management, including risks, actions, issues, decisions, assumptions, owners, and due dates Regulated life-sciences project execution, with working knowledge of regulatory submissions, technical documentation, design controls, QMS, or labeling Project reporting and governance, including milestone tracking, readiness reporting, dashboards, and concise status reporting. Global medical device or IVD registration experience, particularly registration or re-registration programs Product/SKU and country-level data management, including large datasets with multiple regional contributors Power BI or advanced dashboard/reporting capability Workflow automation, such as Power Automate or comparable tools PMP, CAPM, or equivalent project management certification.