This role is dedicated to understanding healthcare regulatory requirements (such as HIPAA, HITRUST, FDA, etc.) and guiding cross-functional teams to systematically integrate those requirements into our SDLC and release management practices. You will work to ensure our processes generate the required documentation, evidence, and compliance packages—ready for both internal use and external audits—primarily through automation and best practices.

  • Proactively identify and interpret relevant healthcare regulatory requirements that impact software development and release management (e.g., HIPAA, HITRUST, FDA).
  • Collaborate with engineering, risk & compliance, cybersecurity, and operations teams to map regulatory requirements to SDLC stages and release workflows.
  • Organize efforts to design, implement, and improve automation for evidence collection, documentation, and compliance package generation throughout the SDLC and release process.
  • Work with product and engineering teams to embed compliance controls, checklists, and documentation templates directly into CI/CD pipelines and release management tools.
  • Serve as a key resource for audit preparation, ensuring our process outputs meet internal and external auditor expectations with minimal manual intervention.
  • Develop executive-level reports and presentations detailing compliance status, risk posture, and process improvements.
  • Foster a culture of process excellence, audit readiness, and automation across all relevant teams and stakeholders.
  • Drive continuous improvement by leveraging feedback, audit findings, and industry best practices.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service