R&D Computer Systems Verification Engineer - Medical Devices

Experis

Little Canada (MN)

On-site

USD 44,000 - 50,000

Full time

3 days ago
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Benefits offered by this job

Weekly Pay
Medical
Dental Plan
Vision Plan
401(k)

Job summary

Experis in Little Canada, MN is seeking a R&D Computer Systems Verification Engineer to join the Healthcare Technology team on a 6-month contract. You will support the Computer Systems Engineering group by developing and executing verification plans for medical device software and hardware components.

The role requires strong attention to detail, documentation, and collaboration with product management, quality, regulatory, and other engineering disciplines to meet delivery objectives.

Qualifications

  • Experience with development and analysis of product requirements
  • Experience with development of test plans, methods, and protocols
  • Experience executing test methods/protocols on hardware and software projects
  • Capable of producing polished, detail-oriented technical documentation
  • Ability to follow written procedures and document progress on tasks

Responsibilities

  • Responsible for the development, qualification, and release of computer system component and software releases for Abbott Electrophysiology Systems
  • Review and develop product requirements, test plans, and test protocols
  • Execute software and computer system verification protocols
  • Enhance and document medical device functionality
  • Collaborate with product management, customer care, quality, regulatory, production, and other engineering disciplines to meet product delivery objectives and business goals

Skills

Requirements development
Test plan creation
Test protocol execution
Technical documentation
Procedural following

Job description

Experis in Little Canada, MN is seeking a R&D Computer Systems Verification Engineer to join the Healthcare Technology team on a 6-month contract. You will support the Computer Systems Engineering group by developing and executing verification plans for medical device software and hardware components.

The role requires strong attention to detail, documentation, and collaboration with product management, quality, regulatory, and other engineering disciplines to meet delivery objectives.

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