RIO Execution Hub (EH) Manager, Sr. Manager

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About the role

JOB SUMMARY   The EH Manager, Sr. Manager is responsible for providing operational regulatory support for designated countries, clusters and/or regions.      This role supports submission logistics and technical aspects, ensuring development and delivery of X-regional, regional and/or national regulatory dossiers from initial application and subsequent lifecycle updates, guaranteeing regulatory compliance throughout the submission process.    It is expected that this role partners closely with the Country Regulatory Strategist (CRS), International Labeling & Artwork (ILA) and other relevant stakeholders as required, to enable timely, high-quality submissions and sustained compliance. This includes but is not limited to:     • Planning regulatory submission timelines ensuring regulatory systems are up to date.  • M1 dossier components (authoring, delivery and/or coordination of local, submission-ready documents), excluding labeling and artwork components.  • Simple local only HA query responses authoring.  • Promptly escalate any submission plan delays and develop mitigation strategies aligned with the assessed impact and associated risks  • The quality review/approval of the Dossier structure for applicable submissions, when required.   • Provide support for general x-functional activities to country Regulatory teams for tenders, out-of-stock reporting, Annual Product Quality Review, risk minimization plans, and coordination of regulatory input for launch planning.  • Identify opportunities to streamline the end-to-end regulatory process, applying digital tools when applicable.    Given the global span of the organization, critical features of this role require strong project management, regulatory operations expertise & digital skills, and the ability to collaborate effectively across diverse cultures, functions, and geographic regions. The individual serves as a trusted partner to global, regional, cluster and local stakeholders, ensuring the timely delivery of high-quality regulatory submissions and operational regulatory support that enables patient access and business objectives.       JOB RESPONSIBILITIES    General responsibilities:    • Leads and coordinates from moderate to complex regulatory submissions (Growth & complex lifecycle) for assigned products aligned with business priorities and needs.  • Accountable for delivering designated tasks with quality and timely as per applicable policy, SOP/Work  Instructions, guidelines, or service level agreement.   • Authors, reviews, and maintains local regulatory documents (Module 1 dossier components) for the submission categories / markets or products assigned.   • Manages and coordinates components receipt, translation management, dossier compilation, local ancillary legalization, and submission readiness to facilitate timely Health Authority submissions.  • Tracks and develops action plans to maintain or improve operational performance against portfolio management, data health, KPI, quality metric, and audit requirement targets for the markets/clusters under responsibility.  • Ensures the timely delivery of high-quality regulatory submissions and dossier components, monitoring them against milestones to meet business-critical timelines and regulatory requirements.  • Manages the authoring of simple HA query responses e.g., admin related requests, and coordinates with relevant SMEs/functions to address more complex HA queries, based on CRS query response strategy.  • Coordinates support to tenders, out-of-stock reporting, Annual Product Quality Reviews, local audit readiness, risk minimization activities, Dear Healthcare Professional Communications (DHPCs), responses to medical information requests and other regulatory operational activities.  • Partners w

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