Senior Quality Assurance Analyst - Regulatory Affairs

Senior Quality Assurance Analyst - Regulatory Affairs Full-time. Compensation: USD 82,500 - USD 110,000 yearly. At Intelerad, we believe the path to answers in healthcare should be clear – whether you are waiting for a diagnosis or trying to expedite one. Our medical imaging solutions streamline the flow of information, simplify complex processes, maximize efficiencies, and shine a light on the unknown. We empower physicians to get patients the answers they need faster and improve outcomes for everyone. With more accessible imaging, we are getting patients out of the dark. Headquartered in Raleigh, NC and Montreal, Intelerad has nearly 800 employees located in offices across four countries. The company empowers nearly 2,000 healthcare organizations around the world with the speed, scalability, and simplicity needed to increase business performance while, most importantly, improving patient outcomes. Intelerad’s modern enterprise solutions have been recognized by a Best in KLAS award, ranking #1 for PACS Asia/Oceania in the 2021 Best in KLAS: Global Software (Non-US) report. The Senior Quality Assurance Analyst (Regulatory Affairs) is responsible for driving quality and compliance excellence across Intelerad’s Software as a Medical Device (SaMD) portfolio. This role combines deep knowledge of medical device quality systems with hands‑on execution of core QA/RA processes, including CAPA, audit readiness, supplier oversight, and regulatory support. As a senior individual contributor within the Regulatory Affairs & Quality organization, this role partners cross‑functionally to ensure quality and regulatory requirements are embedded throughout the product lifecycle and that Intelerad maintains a state of continuous compliance. Key Responsibilities Quality System Execution & Continuous Improvement Lead and manage Corrective and Preventive Actions (CAPAs), including investigations, root cause analysis, effectiveness checks, and documentation. Drive improvements to the Quality Management System (QMS) in alignment with ISO 13485, FDA 21 CFR Part 820, and applicable global regulations. Author, review, and maintain quality system documentation, including SOPs, work instructions, and forms. Track, trend, and analyze quality metrics to identify systemic issues and improvement opportunities. Collaborate with development teams in an Agile environment to integrate quality practices throughout the software development lifecycle. Participate in continuous learning opportunities including training and conferences to stay current with QA methodologies, emerging technologies, and industry best practices. Audit & Inspection Readiness Lead and support internal audits to ensure ongoing compliance with regulatory and internal requirements. Support external audits and inspections (e.g., FDA, Notified Bodies, Health Canada). Coordinate timely responses to audit findings and ensure effective remediation and closure. Supplier & Vendor Quality Management Lead supplier qualification, evaluation, and monitoring activities. Ensure supplier compliance with quality agreements and regulatory expectations. Support supplier audits and ongoing performance assessments. Regulatory Support Support preparation and maintenance of regulatory submissions and registrations for global markets. Participate in regulatory impact assessments, change control, and product lifecycle activities. Collaborate with Regulatory Affairs leadership to support global compliance strategies. Cross‑Functional Collaboration Partner with R&D, Product, Clinical, and Operations teams to integrate quality and regulatory requirements into development and operational processes. Provide guidance on risk management (ISO 14971) and design control expectations. Support complaint handling, post‑market surveillance, and vigilance activities. Required Bachelor’s degree in a scientific, engineering, or healthcare‑related field, or equivalent industry experience. 4+ years of experience in Quality Assurance and/or Regulatory Affairs within the medical device industry. Demonstrated experience working within a certified Quality Management System (ISO 13485). Strong working knowledge of FDA 21 CFR Part 820 / QSR (and QMSR readiness), ISO 13485, and ISO 14971 risk management principles. Proven experience managing CAPA, audits, and supplier quality processes. Strong analytical and problem‑solving skills. Ability to lead quality initiatives and influence cross‑functional stakeholders. Excellent written and verbal communication skills. Strong organizational skills with the ability to manage multiple priorities. Ability to work independently in a regulated, fast‑paced environment. Preferred Experience with electronic QMS platforms (e.g., Greenlight Guru or similar). Prior experience supporting regulatory inspections. Familiarity with global regulatory frameworks (EU MDR, UKCA, Health Canada, TGA, etc.). Quality certifications (e.g., ASQ CQE, CQA). Experience with Software as a Medical Device (SaMD) or healthcare software a major bonus. This job description is not intended to be an exhaustive list of duties, responsibilities, or qualifications and may be modified at any time to meet business needs. All your information will be kept confidential according to EEO guidelines. Applicants may be required to complete an online technical and/or personality assessment as part of your application.

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Intelerad is committed to the principles of equal employment. We are committed to complying with all federal, state and local laws providing equal employment opportunities and all other employment laws and regulations. Applicants, employees and former employees are protected from employment discrimination based on race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability and genetic information (including family medical history). Intelerad is dedicated to the fulfillment of this policy regarding all aspects of employment, including but not limited to recruiting, hiring, placement, transfer, training, promotion, rates of pay, and other compensation, termination, and all other terms, conditions, and privileges of employment. Intelerad is committed to ensuring equal employment opportunity for qualified individuals with disabilities. Intelerad uses the Americans with Disabilities Act (“ADA”) as a standard for global recruiting and hiring purposes. This prohibits discrimination against qualified individuals with disabilities. The ADA defines “disability” as a physical or mental impairment that substantially limits one or more of the major life activities of an individual, a record of such impairment, or being regarded as having such an impairment. By clicking the link above or any third‑party link within this posting, you are leaving this site and going to a third‑party website where the third‑party website’s terms and privacy policy apply. #J-18808-Ljbffr Intelerad