Head of Regulatory Affairs & Quality Control

About the Role

The Head of Regulatory Affairs and Quality Control (RA/QC) is responsible for leading and executing global and domestic regulatory strategy, filings, and compliance activities for AI-driven SaMD products. This role requires a practitioner who not only knows FDA culture and regulatory frameworks, but can also operationalize them, drafting documents, building processes, and coordinating cross-functional activities. Successful candidates will be able to interface with our customer’s regulatory leads to ensure alignment and successful deployment of our AI in the pharma and medtech space. This role reports to the VP of Strategy and will work closely with our , , clinical, and engineering, and LLM model teams.

What You'll Do

Regulatory Strategy & Execution

• Help develop and support regulatory strategies and submissions for AI-enabled SaMD products, including classification, marketing applications (e.g., NDAs, De Novo, 510(k)), and pre-submission pathways.

• Help develop and support regulatory documentation that enables our customers in the pharma and medtech space to meet their compliance obligations when using Hippocratic AI’s products.

• Lead hands-on preparation of regulatory submissions with Legal: drafting sections, coordinating data inputs, managing timelines, and ensuring high-quality documentation.

• Translate regulatory requirements into specific, actionable tasks for clinical, product, engineering, and quality teams.

• Oversee and advance global and domestic regulatory and compliance initiatives, maintaining scientific accuracy, proactively managing risk, and keeping the organization aligned with changing regulatory expectations.

Regulatory Compliance

• Build, manage, and continuously improve a practical regulatory compliance structure across SaMD development lifecycles.

• Collaborate with legal, engineering, clinical, product, and quality teams to ensure compliance with applicable regulations, including 21 CFR Parts 210 and 211, 21 CFR Part 820, SaMD guidance, AI/ML-specific expectations and guidance, cybersecurity, and labeling requirements.

• Help design, support, and maintain a compliant regulatory framework and Pharma-partner guidelines, including iterative AI development, model updates, QMS and GMP requirements, audits and inspections, real-world performance, and post-market monitoring and mitigation.

• Develop and maintain SOPs, controlled documents, audit readiness materials, and inspection response processes.