Quality Engineer || St. Paul Area, Minnesota

Position:

Quality Engineer

• Design Controls & DHF Remediation location: St.

Paul Area, Minnesota (Onsite)

Job Type:

12+ months (Contract)

Job Description:

Focus Areas:

Design Controls Capital Equipment (MEE)

DHF Remediation Project:

Supporting Project Guardian Design Assurance activities Role Overview This role is ideal for a detail‑driven Quality Engineer who thrives in a regulated medical‑device environment and enjoys working at the intersection of design controls, risk management, and product sustaining engineering . You will play a key role in ensuring that Design History Files (DHFs) are complete, compliant, and inspection‑ready while supporting cross‑functional teams in closing documentation gaps and strengthening product quality. You ll contribute directly to the reliability, safety, and compliance of capital equipment products by applying strong design‑control knowledge, risk‑management expertise, and structured problem‑solving. Required Qualifications 3+ years of experience in the medical‑device industry Capital equipment / MEE experience (required) Strong understanding of design controls , including DHF creation and maintenance Experience with Design Inputs/Outputs , specifications, and engineering prints Experience updating and maintaining DFMEA and Hazard Analysis documentation Familiarity with regulated quality systems and documentation practices Key Responsibilities DHF Remediation

• Support gap assessments, evidence collection, and documentation updates to resolve design‑control deficiencies. Remediation Planning
• Help define scope, assumptions, and acceptance criteria for legacy evidence; escalate when additional testing or documentation is required. Design Documentation
• Create or update design inputs/outputs, design reviews, V&V evidence mapping, and traceability matrices. Risk Management
• Lead updates to Hazard Analyses and DFMEAs; ensure alignment between risk controls and remediated DHF content. Traceability
• Support end‑to‑end traceability across inputs, outputs, risk controls, verification, and validation. Cross‑Functional Collaboration
• Work with R D, Manufacturing, Regulatory, and Document Control to route updates and maintain version‑controlled documentation. Audit & Inspection Readiness
• Prepare objective evidence, remediation summaries, and responses to auditor questions. Problem Solving
• Apply structured methodologies to identify and resolve documentation or compliance gaps. Project Support
• Maintain trackers, action‑item logs, and evidence inventories; communicate risks and progress to project leads.

What Success Looks Like Strengthened DHF documentation that is complete, consistent, and inspection‑ready Clear, accurate traceability across design controls and risk‑management elements Smooth collaboration with cross‑functional partners Timely closure of remediation tasks and deliverables Improved compliance posture for capital equipment products Role Expectations & Working Style Knowledge & Expertise You bring strong working knowledge of design controls, risk management, and medical‑device quality systems. You understand how design, manufacturing, and quality intersect-and how documentation supports product safety and compliance. Problem Solving You evaluate complex data sets, identify gaps, and recommend solutions using sound judgment and established quality principles. Planning & Organization You manage non‑routine tasks, maintain schedules, and keep remediation activities on track. Autonomy & Decision‑Making You work under general direction but independently determine approaches, interpret procedures, and recommend improvements. Cross‑Functional Influence You collaborate effectively, communicate with diplomacy, and escalate issues appropriately. Manoj Prajapati | Non-IT Recruiter An•

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