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Design Assurance Engineer (DHF & Risk Management)

APN Consulting IncIndianapolis, IN🇺🇸United StatesPosted 28 Jul 2026

Quick Overview

Work Type
Hybrid
Level
Mid Senior

Job Description

Job Title: Design Assurance Engineer (DHF & Risk Management) 
Location: Indianapolis, IN

 

Role Description: Roles & Responsibilities

  • Support Design History File (DHF) activities for medical device development projects.
  • Review, update, and maintain Global dFMEA documentation, ensuring risks are adequately identified, analyzed, and mitigated.
  • Review, update, and maintain Global uFMEA documentation based on product use scenarios and user-related risks.
  • Develop and update Preliminary Hazard Analysis (PHA) documentation in accordance with risk management procedures.
  • Support the creation and maintenance of product risk management files throughout the product development lifecycle.
  • Prepare, review, and update Product Characterization documents to define product performance and design intent.
  • Create and maintain Product Specification Documents (PSDs), ensuring alignment with design requirements and customer needs.
  • Develop and update Critical-to-Quality (CTQ) documents and establish measurable quality requirements.
  • Support the development and maintenance of Design Input, Design Output, Verification, and Validation documentation.
  • Ensure traceability between user needs, design inputs, risk controls, verification activities, and design outputs.
  • Collaborate with Design, Quality, Regulatory, Manufacturing, and Project Management teams to support product development deliverables.
  • Participate in design reviews and provide technical input on risk management and DHF compliance.
  • Support engineering change assessments and associated documentation updates.
  • Review engineering documents for completeness, accuracy, and compliance with quality system requirements.
  • Identify documentation gaps and recommend corrective actions.
  • Support audits, inspections, and compliance activities related to design control and risk management documentation.
  • Contribute to continuous improvement initiatives for product development and design control processes.
  • Ensure all deliverables comply with applicable regulatory, quality, and Zimmer Biomet procedures, standards, and requirements.
  • Establish document traceability between User Needs, Design Inputs, Design Outputs, Risk Management, Verification, and Validation records within Cockpit Cognition.
  • Support DHF gap assessments, document linking, metadata management, and compliance reviews.
  • Demonstrate familiarity with digital DHF structures, document hierarchies, and traceability matrix development.
  • Support DHF remediation projects and the migration of legacy design documentation into Cockpit Cognition.
  • Communicate project plans, technical direction, and updates effectively (both written and verbal) with personnel across multiple departments.

Essential Skills

  • Strong knowledge of Design History File (DHF) documentation and Design Control requirements.
  • Experience with Design Failure Mode and Effects Analysis (dFMEA) and Use Failure Mode and Effects Analysis (uFMEA).
  • Knowledge of Preliminary Hazard Analysis (PHA) and product risk management processes.
  • Experience preparing and maintaining Product Characterization Documents, Product Specification Documents (PSDs), and Critical-to-Quality (CTQ) documentation.
  • Understanding of Design Inputs, Design Outputs, Verification, Validation, and design traceability.
  • Ability to establish and maintain traceability between User Needs, Design Inputs, Design Outputs, Risk Management, Verification, and Validation documentation.
  • Experience supporting DHF gap assessments, remediation activities, metadata management, document linking, and compliance reviews.
  • Familiarity with Cockpit Cognition and digital DHF document management systems.
  • Knowledge of medical device design control processes and applicable quality and regulatory requirements.
  • Experience working with cross-functional teams, including Design, Quality, Regulatory, Manufacturing, and Project Management.
  • Strong technical documentation, analytical, and organizational skills.
  • Excellent written and verbal communication skills.
  • Ability to manage multiple priorities while maintaining high-quality documentation.
  • Proficiency with Microsoft Office applications, including Word, Excel, and PowerPoint.
  • Strong attention to detail and commitment to documentation accuracy and compliance.

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