Software Verification Engineer

Abbott

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
St. Paul, MN
Salary
$61,300–$122,700 / yr
Employment
Full-time
Posted
2 days ago
Freshness
Confirmed live yesterday

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $196k
This role $92k
$42k most similar roles pay here $245k

This role pays less than 99% of similar roles. Most pay $168,500–$223,000 — the shaded band above. At the midpoint, this role pays about $92k versus about $196k for comparable roles.

Based on 240 similar postings.

Employer

About Abbott

Abbott Laboratories is a global healthcare company that manufactures and markets a broad and diversified line of health care products including diagnostics, medical devices, nutritionals, and branded generic pharmaceuticals. Industry: Healthcare & Medical Devices

Abbott currently has 139 open roles on FindRole.

Listed pay typically runs $86,700–$173,300 across 107 roles with salary data.

Most-posted roles

View all roles at Abbott

At a glance

TL;DR · Software Verification Engineer

Software Verification Engineer II joins the Electrophysiology software verification team to support capital equipment systems. This role involves performing requirements analysis, hazard analysis, and design reviews for new features while ensuring compliance with FDA regulatory and ISO standard procedures. The engineer will be responsible for designing test suites, creating test data, executing test cases, and resolving defects. Day-to-day tasks include debugging code, configuring test systems, and managing the lifecycle of testing artifacts. Technical requirements include proficiency in Linux and Windows operating systems, as well as Python script creation and execution. The candidate must possess experience with software development lifecycle management tools and strong documentation skills to support R&D's ongoing product development. This position focuses on the verification and validation of complex medical device software through automated frameworks, emulators, and rigorous test design for critical healthcare technology.

What you'll do

  • Plan, write, and execute test cases according to FDA regulatory and ISO standard procedures.
  • Perform requirements gathering, hazard analysis, and design reviews for new product features.
  • Design new test suites and identify critical test components for software functionality.
  • Create, update, and execute Linux and Python scripts to support testing activities.
  • Support the implementation and modification of test automation frameworks and tools.
  • Record, track, and resolve defects identified during verification and validation activities.
  • Set up and configure specialized test equipment and systems.
  • Develop and maintain technical documentation and artifacts for the software development lifecycle.

What we're looking for

  • Bachelor's Degree in Engineering (Computer, Electrical, or Software), Computer Science, or a related discipline.
  • 2+ years of professional software test engineering experience.
  • Experience with software development lifecycle management tools.
  • Proficiency in both Windows and LINUX operating systems.
  • Strong technical skills in spreadsheet, word processing, PowerPoint, and specialized applications.
  • Excellent documentation skills to provide information for management decision-making.
  • 2+ months of FDA regulated industry experience (preferred).
  • Polished communicator with strong analytical, organizational, and relationship-building skills (preferred).

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