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Imricor Medical Systems Logo Imricor Medical Systems · IT - Administration

Design Assurance Engineer II

United States, Burnsville Employment contract 80000.00 - 110000.00 USD / Year · Job Posted May 14, 2026
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Job Description

The Design Assurance Engineer II position supports product development to ensure a successful production launch and delivery of the highest quality product to the customer. This position also supports design change and other quality initiatives. This position interacts closely with the Engineering team as well as Operations, Quality Systems, Quality Assurance, Marketing, and Regulatory. This position is responsible for complying with the Imricor Quality Management System requirements and carrying out responsibilities outlined in the environmental, health, and safety policies.

Job Responsibility

  • Executes and supports completion of product development deliverables
  • Creates and supports the development of DHF to ensure content is complete, accurate, and compliant with regulatory standards
  • Supports the development and maintenance of customer requirements, product requirements, and product specifications
  • Collaborates cross-functionally to lead and support completion and maintenance of product risk management deliverables
  • Authors design verification and design validation plan and report documents
  • Implements appropriate sampling inspection and supports qualification activities for purchased components
  • Supports design test method development, and leads method validation activities
  • Utilizes statistical techniques to lead and support characterization, verification, and validation testing and root cause analysis
  • Supports quality system-related deliverables including nonconformances and CAPAs
  • Performs other related duties and responsibilities, as assigned

Requirements

  • Bachelor of Science in Engineering, Science, or technical field
  • 2+ years’ experience in Engineering and/or Quality. Additional education may be substituted for years of experience.
  • Must be able to work independently under limited supervision.
  • Knowledge of basic Quality Systems and good documentation practices.
  • Experience in investigating and implementing Corrective and Preventive Actions
  • Experience in design controls and test method validation
  • Experience with European Medical Device Regulations, FDA 21 CFR Regulations, Australian TGA Regulations, ISO 14971, ISO 13485
  • Advanced computer skills, including statistical/data analysis and protocol/report writing.
  • Strong communication skills, both verbal and written
  • Comfortable working with and seeking optimum solutions with team members in adjacent disciplines of engineering

What we offer

  • Medical
  • Dental
  • Vision
  • Health Savings Accounts
  • Health Care & Dependent Care Flexible Spending Accounts
  • Disability Benefits
  • Life Insurance
  • Retirement Benefits
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