Sr Reliability Engineer

Artech LLC

Minneapolis, MN

JOB DETAILS
SALARY
$55–$60 Per Hour
SKILLS
Code of Federal Regulations, Communication Skills, Continuous Improvement, Cross-Functional, Decision Support, Detail Oriented, Documentation, FDA (Food and Drug Administration), Failure Mode and Effects Analysis (FMEA), File Maintenance, Hazard Analysis, Human Factors, ISO (International Organization for Standardization), Implants, Leadership, Medical Equipment, Medical Records, Patient Assessment, Patient Safety, Product Lifecycle, Product Safety, Reliability Engineering, Risk, Risk Analysis, Risk Management, Statistics, Usability Engineering
LOCATION
Minneapolis, MN
POSTED
7 days ago

Job Title: Sr Reliability Engineer
Job ID: 26689
Location: 7000 Central Ave NE Minneapolis Minnesota 55432
Duration: 12 months
Pay Range: $55.00 - $60.00/HR. on W2


Role Overview

Sr. Risk Engineer responsible for driving and maintaining medical device risk management activities across Class III products. Focus is on ISO 14971 compliance, design controls, and cross-functional risk collaboration throughout the product lifecycle.

Key Responsibilities

  • Maintain and update Risk Management Files for medical devices
  • Perform hazard analysis, FMEA, risk evaluation, and mitigation tracking
  • Ensure risk controls are implemented, verified, and validated
  • Collaborate with Design, Human Factors, Reliability, Safety, and Post-Market teams
  • Assess and document patient safety and product performance risks
  • Support design control deliverables (DV/PV, usability, design transfer, specs)
  • Drive risk process consistency and continuous improvement across projects
  • Communicate risk findings to leadership and stakeholders

Must-Have Skills

  • 3+ years ISO 14971 experience in medical devices
  • Experience maintaining risk management files (Class III preferred)
  • Strong knowledge of design controls / quality design deliverables
  • Experience with hazard analysis, FMEA, risk assessment

Preferred Experience

  • Implantable or complex medical devices
  • FDA 21 CFR 820, ISO 13485, EU MDR knowledge
  • Statistics / risk quantification methods
  • Human factors / usability engineering exposure

Key Competencies

  • Strong cross-functional collaboration & consensus building
  • Attention to detail and documentation accuracy
  • Ability to evaluate and communicate patient risk impacts
  • Leadership in risk discussions and decision-making support

Primary Focus of Role

Ensuring medical devices are safe, compliant, and risk-controlled throughout design and development by managing ISO 14971-based risk files and working closely with engineering and quality teams.

About the Company

A

Artech LLC