Senior Regulatory Affairs Specialist - Onsite

We anticipate the application window for this opening will close on - 31 Oct 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72&#43; million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life The Neurovascular business within Medtronic develops technologies that support the treatment of stroke and other neurovascular conditions. The Regulatory Affairs organization partners across product development, quality, labeling, clinical, and commercial functions to ensure global regulatory compliance and product availability. This role supports regulatory data governance, regulatory process ownership, standards assessments, digital transformation initiatives, and cross-portfolio projects that impact multiple products and regulatory systems across the Neurovascular portfolio. Check us out on LinkedIn: Medtronic Neurovascular . This position is based in Irvine, California, and follows an onsite work model. No travel is required. The Senior Regulatory Affairs Specialist serves as a regulatory subject-matter expert supporting regulatory data integrity, regulatory process excellence, standards assessments, and the implementation of regulatory systems and digital solutions. This role works across multiple product portfolios and regulatory functions to improve data quality, support regulatory initiatives, coordinate cross-functional assessments, and ensure regulatory information is maintained accurately across business systems. Primary Responsibilities Serve as a subject matter expert for regulatory data, related business processes, and regulatory systems across the Neurovascular portfolio. Manage regulatory data governance activities, including data quality reviews, discrepancy resolution, remediation efforts, and continuous improvement initiatives. Coordinate Unique Device Identification (UDI) activities and partner with Regulatory Affairs, Labeling, and cross-functional teams to maintain accurate device registration data. Lead standards gap assessment processes, including assignment, tracking, documentation, stakeholder coordination, and completion of required actions. Coordinate regulatory change assessments and evaluate potential impacts across products, regions, registrations, and regulatory systems. Lead or support cross-functional regulatory projects involving multiple products, product families, or regulatory teams. Support implementation, testing, validation, migration, reconciliation, and verification activities for regulatory systems and digital solutions. Partner with business and corporate stakeholders to implement process improvements, automation opportunities, and AI-enabled regulatory initiatives. Required Qualifications Bachelor's degree and 4&#43; years of regulatory affairs, quality, standards, or medical device experience OR Advanced degree and 2&#43; years of regulatory affairs, quality, standards, or medical device experience. Experience managing projects, processes, or initiatives involving multiple stakeholders, products, or regulatory systems. Experience coordinating standards assessments and driving actions to completion with Regulatory Affairs and cross-functional subject matter experts. Experience evaluating regulatory impacts and maintaining compliance-related documentation, data, or business processes. Experience working within regulated medical device environments. Preferred Qualifications Experience with Unique Device Identification (UDI), global device registrations, EUDAMED, regulatory information management systems, or data governance. Experience supporting digital transformation, automation, analytics, or AI-enabled initiatives in a regulated environment. Experience assessing the regulatory impact of standards updates across product portfolios and supporting related change assessments. Experience leading cross-functional projects involving regulatory systems, process improvements, or enterprise initiatives. Knowledge of global medical device regulatory requirements, registrations, and product lifecycle management processes. For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. 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