Senior Regulatory Affairs Specialist
WHO WE ARE:
NeuroLogica Corp., a subsidiary of Samsung Electronics Co. Ltd., develops, manufactures, and markets innovative imaging technologies and is committed to delivering fast, easy, and accurate diagnostic solutions to healthcare providers. NeuroLogica is the global corporate headquarters and manufacturer of mobile computed tomography, and is also the US headquarters for sales, marketing, service and distribution of all Samsung digital radiography and ultrasound systems. Our advanced medical technologies are used worldwide in leading healthcare institutions, helping providers enhance patient care, improve patient satisfaction, and increase workflow efficiency. Samsung is committed to being a leader in the field of healthcare imaging.
Samsung is a growing presence in the radiology field and is committed to delivering fast, easy and accurate imaging solutions to healthcare providers. In 2015, NeuroLogica became the US headquarters for all of Samsung Health and Medical Equipment. The full range of Samsung imaging solutions includes Ultrasound, Digital Radiography, and mobile Computed Tomography (mCT). Samsung aims to become a global leader in the medical imaging space and is investing heavily in developing innovative, advanced imaging technologies that will improve the quality of people's lives.
Samsung keeps a constant eye on the always-evolving, ever-changing imaging industry. By continually enhancing current product lines and seeking to develop new technologies, Samsung is at the forefront of the imaging frontier.
ROLE DESCRIPTION:
Responsible for leading and executing global regulatory submissions and compliance activities for our innovative portfolio of ultrasound, AI-enabled imaging, CT, and digital X-ray medical devices.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned
Manage end-to-end process AI-enabled medical devices including data collection, model performance and monitoring on safety and effectiveness Work cross functionally to ensure all AI systems from large language models (LLMs) to multimodal architectures have appropriate data management practices for training, tuning and testingLead the planning, preparation, and submission of regulatory dossiers, including FDA 510(k), De Novo, EU MDR Technical Documentation, Health Canada license applications, ANVISA, NMPA, CDSCO, TGA, and other international filings.Develop and execute regulatory strategies for new product development, AI/ML-enabled imaging software, SaMD and legacy product lifecycle managementBuild creative, scalable solutions for managing large image databases and supporting submission workflowsWork with, and respond to, inquiries from regulatory agencies including FDA, EU Notified Body, NMPA, PMDA, TGA, ANVISA and other national and regional health authoritiesSupport post-market surveillance, vigilance reporting, change assessmentsMonitor the regulatory environment. Stay abreast of changes in regulations throughout all major international geographies and disseminate new regulations and guidance to members of R&Q, Product, Engineering and MarketingMaintain dashboard for regulatory approvals for international country license / registration renewalsReview labeling and promotional materials to ensure consistency with regulatory approvalsLead cross functional teams with Product, Marketing, Engineering, Clinical to prepare and secure timely product approvals, clearance and registrationsProvide assistance and expertise during regulatory inspectionsPromote teamwork and collaboration within the regulatory function and with other functional areasAbility to create regulatory updates for Management Review MeetingCommunicate clearly (written and oral) with other company personnel, vendors, regulatory agencies, auditors, and the customer as requiredWork independently with minimal supervision and as part of team Keep knowledge of all NeuroLogica products up-to-dateFollow all company policies regarding training, travel, expenses, meetings, and mealsManage time effectively; prioritize and make good business judgments and decisions in relationship to efficiency, effectiveness
EDUCATION & EXPERIENCE
Bachelor’s in Regulatory, Engineering or related field preferred5+ years of related experience in regulatory affairs Proven track record of authoring successful submissions of FDA 510(k)sCE Marking and other international registrationsPost-market regulations and requirements for medical devicesWorking with devices involving CT, X-Ray and Ultrasound.Regulatory Affairs Certification (RAC) preferred. Strong knowledge of international medical device regulations (FDA, Health Canada, ANVISA, NMPA, CDSCO, TGA)Familiarity with AI/ML regulatory frameworks, cybersecurity and usability standardsAbility 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 deadlinesTechnically savvy; must be able to discuss, understand and author presentations, documentation and reportsExcellent written, oral, and documentation skillsIn compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire
COMPUTER & ANALYTIC SKILLS
Must be able to assemble facts from various areas, analyze data, and provide informed recommendations to managementMust be able to work with minimal supervision, take charge of projects, and work effectively in a demanding, fast paced environmentMust 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
PHYSICAL REQUIREMENTS
Occasionally lift and /or move up to 25 poundsFrequently required to sit; use hands to finger, handle, or feel; reach with hands; and talk or hearMust 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 focusInteraction 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
COMPETENCIES
High attention to detailUnderstanding of terminology and ability to share and communicate effectively within the groupAbility to organize and prioritize tasks resulting in consistent productivityAbility to function within and support a team environment and build strong working relationshipsDependable and punctualAbility to meet accuracy and productivity goals.Good problem-solving skills, ability to evaluate situation and prioritize factors in decision makingSelf-motivated, utilize available resources for self-improvement and developmentFlexible: able to follow directives and accomplish tasks outside of normal duties
About NeuroLogica
Located North of Boston in Danvers, MA, NeuroLogica Corporation, a subsidiary of Samsung Electronics, develops, manufactures and markets innovative medical imaging equipment for healthcare facilities and private practices worldwide. As a fast-moving, entrepreneurial company, NeuroLogica is a rapidly growing presence in the radiology field and is committed to delivering fast, easy and accurate imaging solutions to healthcare providers. We welcome you to learn more at:
https://www.neurologica.com .
We offer a comprehensive benefit package which includes;
- 4 Different Blue Cross/Blue Shield Medical Plans to meet your needs
- Dental coverage through BlueCross/Blue Shield Dental
- Vision coverage by Blue Cross/Blue Shield
- Company paid Short-term and Long-term Disability coverage
- $1 for $1 401k match up to 5% managed by Fidelity
- Other benefit options such as company paid employee life insurance, a wellness program, tuition reimbursement and many more!
NeuroLogica welcomes diversity and is an AA/EEO Employer – Minorities/Women/Veterans/Disabled and other protected categories are always encouraged to apply.
