AI Regulatory Manager

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. AI Regulatory Manager W2 Regular Full Time Danvers, MA, US 3 days ago Requisition ID: 1101 Who We Are Samsung HME America (Healthcare and Medical Equipment) is Samsung’s U.S. medical imaging organization, delivering advanced diagnostic solutions across Ultrasound, Digital Radiography, and Computed Tomography. We lead nationwide sales, marketing, service, and distribution of Samsung’s imaging technologies, partnering with healthcare providers to strengthen diagnostic capabilities, streamline clinical workflows, and support better patient care. Samsung HME America also serves as the global manufacturing center for Samsung’s mobile Computed Tomography (mCT) business, leading the development of advanced CT systems used by healthcare providers worldwide. Backed by Samsung Electronics’ global technology leadership, our teams work closely with clinicians to translate real-world challenges into innovative imaging solutions. Our culture combines a sense of urgency, customer focus, and clinical collaboration to advance the future of medical imaging. Role Description The AI Regulatory Manager will be the principal architect of regulatory strategy and execution for our AI/ML-enabled imaging and software-as-a-medical-device (SaMD) portfolio catering to ultrasound, CT, and digital X-ray medical devices. This individual will be responsible for developing and implementing regulatory strategies, preparing and managing complex submissions and ensuring compliance with evolving global regulations and standards. Key duties and responsibilities Lead the end-to-end regulatory lifecycle for AI-enabled medical devices, including data collection, model performance evaluation, safety and effectiveness monitoring, and post-market surveillance. Define and implement regulatory strategies for AI/ML-driven imaging software, SaMD, and legacy imaging products, across all stages from concept to post-market. Partner with Product, Marketing, Engineering, Clinical to prepare and secure timely product approvals, clearance and registrations Oversee planning, preparation, and submission of regulatory dossiers, including FDA 510(k), EU MDR Technical Documentation, Health Canada, ANVISA, NMPA, CDSCO, TGA, and other international filings. Maintain dashboards for global regulatory approvals, license and registration renewals, labeling and promotional material compliance, and support management review and strategic planning. Provide assistance and expertise during regulatory inspections Build and maintain scalable frameworks for managing large imaging- and data-sets (training, tuning, test sets), regulatory documentation, and submission workflows. Mentor, coach, and manage junior regulatory and AI-staff; build regulatory-AI competence within the organization. Communicate clearly (written and oral) with other company personnel, vendors, regulatory agencies, auditors, and the customer as required Work independently with minimal supervision and as part of team Maintain current knowledge of Samsung HME America products Qualifications and Requirements To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Education & Experience Bachelor’s in Regulatory, Engineering or related field preferred 8+ years of progressive regulatory affairs experience in medical devices, with at least 3–5 years directly managing AI/ML–enabled imaging software or SaMD product regulatory work. Proven track record of authoring successful submissions of FDA 510(k)s CE Marking and other international registrations Management of AI-enabled medical devices Working with devices involving CT, X-Ray and Ultrasound. Strong knowledge of global medical device regulations — FDA, EU MDR, ISO 13485, and relevant standards for AI/ML software, cybersecurity, usability, and post-market Regulatory Affairs Certification (RAC) preferred Ability to communicate effectively with engineers, marketing, and management through all media Strong organizational and project management skills, with the ability to manage multiple priorities and deadlines Technically savvy; must be able to discuss, understand and author presentations, documentation and reports Excellent written, oral, and documentation skills Computer & Analytical Skills Must be able to assemble facts from various areas, analyze data, and provide informed recommendations to management Must be able to work with minimal supervision, take charge of projects, and work effectively in a demanding, fast paced environment Must be excellent with technology, be able to present using a laptop computer, and be able demonstrate proficiency with MS Office package, including Excel, Word, and PowerPoint, as well as Outlook High attention to detail Skilled in leading teams, motivating staff and building quality culture. Ability to meet accuracy and productivity goals Good problem solving skills, ability to evaluate situation and prioritize factors in decision making Self-motivated, utilize available resources for self-improvement and development Flexible: able to follow directives and accomplish tasks outside of normal duties Physical Requirements Working flexible hours to accommodate global time zones Frequently required to sit; use hands to finger, handle, or feel; reach with hands; and talk or hear Must be able to sit for long periods of time The noise level in the work environment is usually mild. Specific vision abilities required by this job include Close vision, Distance vision, Peripheral vision, Depth perception and Ability to adjust focus Interaction with x-ray devices; for this reason strict safety and tracking programs are in place, requiring the utilization of dose monitoring equipment either full time or as necessitated by situation We offer a comprehensive benefit package which includes: Medical (Blue Cross Blue Shield): 5 PPO Plans (with up to 95% employer contribution) Dental (Blue Cross Blue Shield): 2 PPO Plans (with up to 80% employer contribution) Short/Long Term Disability, Life & AD&D (The Standard):100% company paid 401k Retirement (Fidelity):100% company match up to 5% Tax Deferred Health Care Savings Programs Accident Insurance, Critical Illness, Hospital Indemnity, Pet, Legal, ID Theft Generous paid time off, tuition reimbursement, and more! Inclusion and Diversity Statement We are an Equal Opportunity Employer and value diversity at all levels of the organization. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or any other characteristic protected by applicable law. We are committed to providing reasonable accommodation to individuals with disabilities throughout the application and employment process. If you require assistance or accommodation, please contact Human Resources. #J-18808-Ljbffr NeuroLogica Corp.