Manager - Registration Management

Responsibilities

• Lead and develop a high-performing RIMs team to deliver seamless day-to-day regulatory operations
• Oversee the creation and maintenance of regulatory applications for NPIs, safety variations, and lifecycle activities
• Provide subject-matter expertise and operational support for regulatory activities managed within centralized RIMs systems
• Manage workflows for the timely delivery of critical regulatory reports supporting supply, manufacturing, and PV inspections
• Own XeVMPD submissions and ensure the ongoing maintenance of registered product data
• Ensure accuracy, integrity, and completeness of registered product and master data across global markets
• Maintain and update SOPs and Work Instructions to ensure continuous audit and inspection readiness
• Support regulatory audits and health authority inspections through RIMs expertise and data extraction
• Lead User Acceptance Testing (UAT) for new features, system enhancements, or major RIMs implementations
• Drive continuous improvement, data quality excellence, and compliance with global regulatory requirements
• Manage team performance, capability building, and career development

Requirements

• Strong knowledge of global regulatory regulations and guidelines
• Hands-on experience with industry-standard RIMs tools and regulatory systems
• Proven people leadership and stakeholder management capability

About the Company

Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions across the spectrum of health, around the world, for all stages of life.