Responsible for the collection, coordination, and summary of global regulatory intelligence that pertains to the company and our portfolio. Manage internal intelligence communications and act as SME for RI database; collaborate with global partners to coordinate and collect updates from their specific regions. Essential Job Duties. Solid understanding of how to analyze regulatory intelligence and translate it into clear implications for product development, clinical strategy, submissions, and lifecycle management. Help establish and refine internal regulatory intelligence processes and best practices. Evaluate and implement tools, databases, or systems that enhance regulatory intelligence capabilities. Contribute to continuous improvement of Reg Intel processes. Develop internal communications, training materials, and presentations to keep teams informed of relevant intelligence updates. Assist RI Leader in building a culture of regulatory awareness across the organization. Qualifications. Required Experience and Education. Minimum 5 years of experience in regulatory affairs and bachelor’s degree in a relevant discipline, or equivalent combination ofeducation and experience. Demonstrated ability to interpret complex regulatory information and translate it into business impact. Required Knowledge, Skills and Abilities. Project management abilities. Strong written and verbal communication. Project coordination and time management skills. Strong analytical and problem-solving skills. Ability to interpret and translate complex topics into simple language without losing context. Competence with document management systems and Microsoft Office. Preferred Knowledge, Skills and Abilities. Experience supporting innovative technologies such as surgical robotics, digital health, or complex medical devices. Familiarity with global regulatory pathways and evolving regulatory frameworks. Physical Requirements. Not applicable