Senior Quality Assurance Engineer

Job Summary

The Senior Quality Assurance Engineer (Design Assurance) is responsible for providing oversight and governance of Design History Files (DHF) to ensure compliance with regulatory standards and internal quality requirements. This role plays a key part in guiding design controls, facilitating design transfer, and managing risk documentation across medical device product lines (Class I and Class II 510(k)). The engineer will ensure that all processes and documentation meet FDA and ISO standards, and that design changes are properly controlled and documented.

• Conduct end-to-end DHF audit and gap assessment, including:
  • Design & Development Plan
  • User Needs
  • Design Inputs & Outputs
  • Design Verification & Validation (V&V)
  • Risk Management Files (ISO 14971)
  • Design Reviews and Traceability
• Evaluate traceability across DHF elements (Inputs → Outputs → V&V → Risk)
• Identify missing, weak, or non‑compliant documentation
• Deliver audit‑defensible gap assessment reports with actionable remediation recommendations
• Assess regulatory gaps versus procedural non‑conformities
• Work with partially remediated or legacy DHFs

• Strong expertise in Medical Device Design Controls (21 CFR 820.30, ISO 13485)
• Hands‑on experience in reviewing and auditing DHFs (not just document authoring)
• In‑depth knowledge of ISO 14971 risk management (hazards, controls, residual risk)
• Experience supporting DHF remediation in response to regulatory compliance gaps
• Strong ability to assess traceability and consistency across documentation
• Senior‑level Quality or Regulatory professional
• Prior experience as DHF Auditor / Reviewer, Design Controls SME, Quality Engineer in FDA‑regulated medical devices
• Ability to work independently and communicate findings clearly
• Strong documentation and report‑writing skills
• Focus is on analysis and gap identification, not document rewriting