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AI Regulatory Manager

35bc48a5 5c30 4e17 B7c3 4b6c00cc84dd 9202192235070 2 · Danvers, MA, US, Danvers, MA · Active · ADP Workforce Now Recruiting

Job facts

FieldValue
Company35bc48a5 5c30 4e17 B7c3 4b6c00cc84dd 9202192235070 2
TitleAI Regulatory Manager
Normalized title-
Department / team-
LocationDanvers, MA, United States
Work model-
Employment typeFull Time
Salary-
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-04-19 / 2026-05-31
Changed / last seen2026-06-19 / 2026-06-19

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Linked records

Company35bc48a5 5c30 4e17 B7c3 4b6c00cc84dd 9202192235070 2
Sourcec663b262-9b67-4fc5-ac34-cee542514605
ATS providerADP Workforce Now Recruiting

Description

AI Regulatory Manager Location: Danvers, MA 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, other duties may be assigned: 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 Competencies 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 Benefits 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 ) Vision (Blue Cross Blue Shield): 100% company paid 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.

Full job record

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Last Seen At2026-06-19 12:35:51Z
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    "requisitionDescription": "<div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div id=\"isPasted\"><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;' data-pasted=\"true\"><strong><span style=\"font-size: 19px; font-family: Roboto; color: rgb(0, 0, 0);\">AI Regulatory Manager</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style=\"font-size: 19px; font-family: Roboto; color: rgb(0, 0, 0);\">Location: &nbsp;Danvers, MA</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style=\"font-family:Roboto;color:#75787B;\">&nbsp;</span></strong></p><p style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; text-align: justify;\"><strong><span style=\"font-size:19px;font-family:Roboto;color:#1428A0;\">Who We Are</span></strong></p><p><span style='font-family: \"times new roman\", serif; font-size: 16px; color: rgb(0, 0, 0);'>Samsung HME America (Healthcare and Medical Equipment) is Samsung&rsquo;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&rsquo;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&rsquo;s mobile Computed Tomography (mCT) business, leading the development of advanced CT systems used by healthcare providers worldwide.</span></p><p><span style='font-family: \"times new roman\", serif; font-size: 16px; color: rgb(0, 0, 0);'>Backed by Samsung Electronics&rsquo; 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.</span></p><p style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; text-align: justify;\"><strong><span style=\"font-size:19px;font-family:Roboto;color:#1428A0;\">Role Description</span></strong></p><p style=\"margin-left: 0in; line-height: 1.15;\" data-pasted=\"true\"><span style='font-family: \"times new roman\", serif; font-size: 16px;'>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.&nbsp;</span><strong><span style=\"font-family:Roboto;color:#75787B;\"> </span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;' data-pasted=\"true\"><strong><span style=\"font-size:19px;font-family:Roboto;color:#1428A0;\">Key duties and responsibilities,</span></strong><span style=\"font-family:Roboto;color:#75787B;\">&nbsp;</span><span style=\"font-family: Roboto; color: rgb(0, 0, 0);\">other duties may be assigned:</span></p><ul><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>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.&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Define and implement regulatory strategies for AI/ML-driven imaging software, SaMD, and legacy imaging products, across all stages from concept to post-market.&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Partner with Product, Marketing, Engineering, Clinical to prepare and secure timely product approvals, clearance and registrations&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>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.&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Maintain dashboards for global regulatory approvals, license and registration renewals, labeling and promotional material compliance, and support management review and strategic planning.&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Provide assistance and expertise during regulatory inspections&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Build and maintain scalable frameworks for managing large imaging- and data-sets (training, tuning, test sets), regulatory documentation, and submission workflows.&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Mentor, coach, and manage junior regulatory and AI-staff; build regulatory-AI competence within the organization.&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Communicate clearly (written and oral) with other company personnel, vendors, regulatory agencies, auditors, and the customer as required&nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Work independently with minimal supervision and as part of team &nbsp;</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15;'>Maintain current knowledge of Samsung HME America products</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><br></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;text-align:justify;background:white;' data-pasted=\"true\"><strong><span style=\"font-size:19px;font-family:Roboto;color:#1428A0;\">Qualifications and Requirements:</span></strong><strong><span style=\"font-family:Roboto;color:#75787B;\"> </span></strong><span style=\"font-family: Roboto; color: rgb(0, 0, 0);\">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.</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family:Roboto;color:#75787B;\">&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style=\"font-family:Roboto;color:#1428A0;\">Education &amp; Experience</span></strong></p><ul><li style='line-height: 1.15; font-family: \"times new roman\", serif; font-size: 16px;'>Bachelor&rsquo;s in Regulatory, Engineering or related field preferred&nbsp;</li><li style='line-height: 1.15; font-family: \"times new roman\", serif; font-size: 16px;'>8+ years of progressive regulatory affairs experience in medical devices, with at least 3&ndash;5 years directly managing AI/ML&ndash;enabled imaging software or SaMD product regulatory work.&nbsp;</li><li style='line-height: 1.15; font-family: \"times new roman\", serif; font-size: 16px;'>Proven track record of authoring successful submissions of FDA 510(k)s&nbsp;</li><li style='font-family: \"times new roman\", serif; line-height: 1.15; font-size: 16px;'>CE Marking and other international registrations</li><li style='font-family: \"times new roman\", serif; line-height: 1.15; font-size: 16px;'>Management of AI-enabled medical devices</li><li style='font-family: \"times new roman\", serif; line-height: 1.15; font-size: 16px;'>Working with devices involving CT, X-Ray and Ultrasound.</li><li style='font-family: \"times new roman\", serif; line-height: 1.15; font-size: 16px;'>Strong knowledge of global medical device regulations &mdash; FDA, EU MDR, ISO 13485, and relevant standards for AI/ML software, cybersecurity, usability, and post-market</li><li style='font-family: \"times new roman\", serif; line-height: 1.15; font-size: 16px;'>Regulatory Affairs Certification (RAC) preferred</li><li style='font-family: \"times new roman\", serif; line-height: 1.15; font-size: 16px;'>Ability to communicate effectively with engineers, marketing, and management through all media </li><li style='font-family: \"times new roman\", serif; line-height: 1.15; font-size: 16px;'>Strong organizational and project management skills, with the ability to manage multiple priorities and deadlines</li><li style='font-family: \"times new roman\", serif; line-height: 1.15; font-size: 16px;'>Technically savvy; must be able to discuss, understand and author presentations, documentation and reports</li><li style='font-family: \"times new roman\", serif; line-height: 1.15;'><span style=\"font-size: 16px;\">Excellent written, oral, and documentation skills</span>&nbsp;</li></ul><p style=\"margin-top: 0in; margin-right: 0in; margin-bottom: 0in; line-height: 1.15; font-size: 16px; font-family: Aptos, sans-serif;\"><span style='font-family: \"times new roman\", serif; color: rgb(117, 120, 123); font-size: 16px;'>&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;' data-pasted=\"true\"><strong><span style=\"font-family:Roboto;color:#1428A0;\">Computer &amp; Analytical Skills</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><br></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0); background: white;\"><span style=\"font-family: Roboto;\">Must be able to assemble facts from various areas, analyze data, and provide informed recommendations to management</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0); background: white;\"><span style=\"font-family: Roboto;\">Must be able to work with minimal supervision, take charge of projects, and work effectively in a demanding, fast paced environment</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0); background: white;\"><span style=\"font-family: Roboto;\">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</span></li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;background:white;'><strong><span style=\"font-family:Roboto;color:#75787B;\">&nbsp;</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;' data-pasted=\"true\"><strong><span style=\"font-family:Roboto;color:#1428A0;\">Competencies</span></strong></p><ul><li style='margin-top: 0in; margin-right: 0in; margin-bottom: 0in; line-height: normal; font-size: 16px; font-family: \"times new roman\", serif; color: rgb(0, 0, 0);'>High attention to detail</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15; color: rgb(0, 0, 0);'>Skilled in leading teams, motivating staff and building quality culture.</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15; color: rgb(0, 0, 0);'>Ability to meet accuracy and productivity goals</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15; color: rgb(0, 0, 0);'>Good problem solving skills, ability to evaluate situation and prioritize factors in decision making</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15; color: rgb(0, 0, 0);'>Self-motivated, utilize available resources for self-improvement and development</li><li style='font-family: \"times new roman\", serif; font-size: 16px; line-height: 1.15; color: rgb(0, 0, 0);'>Flexible: able to follow directives and accomplish tasks outside of normal duties</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style=\"font-family:Roboto;color:#1428A0;\">Physical Requirements</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><br></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Working flexible hours to accommodate global time zones&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Frequently required to sit; use hands to finger, handle, or feel; reach with hands; and talk or hear</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Must be able to sit for long periods of time&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">The noise level in the work environment is usually mild.</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Specific vision abilities required by this job include Close vision, Distance vision, Peripheral vision, Depth perception and Ability to adjust focus</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">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</span></li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style=\"font-family:Roboto;color:#75787B;\">&nbsp;</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><strong><span style=\"font-size:19px;font-family:Roboto;color:#1428A0;\">Benefits</span></strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: Roboto; color: rgb(0, 0, 0);\">We offer a comprehensive benefit package which includes:</span></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Medical (Blue Cross Blue Shield): 5 PPO Plans (<em>with up to 95% employer contribution</em>)</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Dental (Blue Cross Blue Shield): 2 PPO Plans (<em>with up to 80% employer contribution</em>)</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Vision (Blue Cross Blue Shield):&nbsp;100% company paid</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Short/Long Term Disability, Life &amp; AD&amp;D (The Standard):&nbsp;100% company paid</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">401k Retirement (Fidelity):&nbsp;100% company match up to 5%</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Tax Deferred Health Care Savings Programs</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Accident Insurance, Critical Illness, Hospital Indemnity, Pet, Legal, ID Theft&nbsp;</span></li><li style=\"margin: 0in; line-height: normal; font-size: 16px; font-family: Aptos, sans-serif; color: rgb(0, 0, 0);\"><span style=\"font-family: Roboto;\">Generous paid time off, tuition reimbursement, and more!</span></li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.25in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family:Roboto;color:#75787B;\">&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;text-align:justify;'><strong><span style=\"font-family:Roboto;color:#1428A0;\">Inclusion and Diversity Statement: </span></strong><span style=\"font-family: Roboto; color: rgb(0, 0, 0);\">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.</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;line-height:normal;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family:Roboto;color:#75787B;\">&nbsp;</span></p></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div>\n",
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