Director of Quality and Regulatory Affairs (Remote)

Position SummaryThe Director of Quality and Regulatory Affairs will report directly to the CEO and be responsible for developing, implementing, and maintaining quality systems and regulatory compliance processes in accordance with FDA regulations (21 CFR Part 820) and ISO 13485 standards. This role will own the Quality Management System (QMS) and ensure compliance across design, development, manufacturing, and post-market surveillance activities. The position will serve as the primary contact during regulatory inspections and notified body audits and is critical to ensuring the safety, efficacy, and compliance of SleepRes' sleep and respiratory medical devices.Core CompetenciesQuality Management System (QMS)Design Controls (DHF, DMR, DHR)510(k) submissions and regulatory consultant collaborationFDA inspections and ISO 13485 auditsISO 14971 risk managementCAPA managementSupplier quality and incoming inspectionClass II and Class III medical device complianceComplaint handling and post-market surveillanceValidation (IQ/OQ/PQ)Regulatory compliance strategyRequirements (Must-Have)7+ years of experience in Quality Assurance and Regulatory Affairs within the medical device industry.Experience working with Class II medical devices or higher (Class II, II+, or Class III). Experience preparing and submitting 510(k) submissions, including collaboration with regulatory consultants. Strong knowledge of 21 CFR Part 820, ISO 13485, and ISO 14971. Experience leading FDA inspections or ISO 1345 audits. Hands-on experience with Design Controls, CAPA, risk management, and post-market surveillance. People management and cross-functional leadership experience. Preferred QualificationsExperience with respiratory devices or CPAP systems.Early-stage startup experience. Experience with electronic QMS (eQMS) systems. RAC certification or advanced degree in a related field. Key ResponsibilitiesQuality ManagementOversee and manage the quality organization, including design assurance, manufacturing quality, customer feedback, supplier management, and audit compliance. Establish and maintain Key Process Indicators (KPIs) to measure quality performance and drive continuous improvement. Lead management reviews and ensure alignment with quality goals and objectives.Own the Design Control process (21 CFR 820.30), ensuring proper documentation of DHF, DMR, and DHR. Establish incoming inspection and supplier quality processes, including qualification, monitoring, and audits. Develop and maintain quality documentation including SOPs, Work Instructions, and quality records. Oversee complaint handling, MDR evaluation, and post-market surveillance processes. Regulatory AffairsNavigate the global regulatory landscape to ensure successful product approvals in various markets.Develop regulatory strategy for new products, modifications, and international market entry (EU MDR, Health Canada, etc.). Prepare regulatory filings, including 510(k) submissions and PMAs, with support from regulatory consultants as needed. Maintain regulatory documentation, including Technical Files and 510(k)/PMA support documents. Manage interactions with the FDA, including Q-Sub meetings and audits. Review and approve labeling, IFU, claims, and marketing materials for regulatory compliance. Implement regulatory compliance strategy across the product lifecycle.Team LeadershipLead and develop a high-performing quality and regulatory affairs team. Mentor team members on best practices in quality assurance and regulatory compliance. Partner closely with Engineering, Clinical, and Operations to integrate quality and regulatory requirements into product development. Audit and ComplianceConduct internal audits to verify compliance with quality standards and regulatory requirements. Work with Notified Bodies to establish and maintain ISO 13485 compliance. Manage CAPA processes to address non-conformities and improve product quality.Serve as Management Representative for ISO 13485 and FDA Quality System Regulation. Risk ManagementImplement risk management strategies to identify and mitigate medical device hazards. Ensure compliance with ISO 14971 risk management requirements. Ensure risk assessments are conducted across the product development process. Lead post-market risk evaluation and field corrective actions when required. SkillsStrong understanding of FDA regulations, ISO 13485, and global regulatory requirements. Excellent leadership, communication, and interpersonal skills.Ability to work collaboratively across departments and regulatory agencies. Strong analytical and documentation skills, including validation protocol development (IQ/OQ/PQ). Experience with electronic QMS systems preferred. Ability to operate effectively in a fast-paced startup environment. Work EnvironmentThis role operates in a fast-paced, innovative startup environment requiring adaptability and proactive problem-solving skills. The Director will establish structure and discipline while supporting rapid development and iteration.Some travel may be required for audits, supplier visits, and regulatory meetings. Apply tot his job