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Software Validation Jobs in Minnesota (NOW HIRING)

Hahn Group

Controls Engineer, Software

Brooklyn Park, MN · On-site

$47.25 - $60.25/hr

... validation protocols to confirm the machine control software meets all safety, performance, and technical requirements Share with department staff the design methodologies, productivity tools ...

UnitedHealth Group

Software Engineer

Eden Prairie, MN · Remote

$72K - $130K/yr

Perform comprehensive software validation, performance testing, and verification testing to ensure enterprise-grade reliability * Document development phases, establish system monitoring, and ensure ...

UnitedHealth Group

Software Engineer

Eden Prairie, MN · On-site

$72K - $130K/yr

Perform comprehensive software validation, performance testing, and verification testing to ensure enterprise-grade reliability * Document development phases, establish system monitoring, and ensure ...

Collabera

Manufacturing Engineer

Columbia Heights, MN

$74K - $95K/yr

Perform Equipment Installation, Mfg Process Characterization, Operational Qualification, and Performance Qualification (IQ/OQ/PQ) activities, as well as Software Validation and Test Method Validation ...

Danaher

Manager Quality Assurance, Validation

Chaska, MN · On-site

$130K - $160K/yr

Experience with non-product software validation for manufacturing automation * Manufacturing process validation experience - medical device or pharmacy industry highly preferred * Experience with ...

AGCO

Validation Engineer

Jackson, MN

$54K - $100K/yr

Our work is tightly integrated with validation teams to ensure designs meet functional and ... Minimum of 1 year of hands-on experience using 3D CAD software (CREO), along with NVH testing and ...

AGCO

Validation Engineer

Jackson, MN · On-site

$54K - $100K/yr

Our work is tightly integrated with validation teams to ensure designs meet functional and ... Minimum of 1 year of hands-on experience using 3D CAD software (CREO), along with NVH testing and ...

AGCO

Validation Engineer

Jackson, MN · On-site

$54K - $100K/yr

Our work is tightly integrated with validation teams to ensure designs meet functional and ... Minimum of 1 year of hands-on experience using 3D CAD software (CREO), along with NVH testing and ...

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Software Validation information

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$10

$55

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How much do software validation jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for software validation in Minnesota is $55.15, according to ZipRecruiter salary data. Most workers in this role earn between $40.72 and $68.99 per hour, depending on experience, location, and employer.

What does software validation do?

In a Software Validation role, your day typically involves developing and executing test cases, identifying and documenting software defects, and collaborating closely with development and quality assurance teams. You may also participate in requirement reviews, create validation reports, and ensure that software meets specified regulatory or industry standards. Many roles involve a mix of manual and automated testing tasks to comprehensively assess software performance and functionality. Regular communication with cross-functional teams is vital to resolve issues quickly and maintain product quality. This dynamic environment provides continuous learning and development opportunities, especially as new tools and standards are adopted.

What are the key skills and qualifications needed to thrive in software validation?

To thrive as a Software Validation professional, you need a solid understanding of software testing principles, validation methodologies, and quality assurance processes, often complemented by a degree in computer science, engineering, or a related field. Familiarity with test automation tools (such as Selenium or JUnit), validation frameworks, and compliance standards like ISO or FDA regulations is highly valuable. Attention to detail, analytical thinking, and effective communication skills help professionals excel in this role. These competencies are essential to ensure the reliability, safety, and compliance of software products before they reach end users.

What is software validation?

A Software Validation job involves ensuring that software meets its intended purpose and complies with regulatory or industry standards. Professionals in this role design and execute test plans, document findings, and work closely with developers to resolve issues. This position is common in industries like healthcare, automotive, and finance, where software reliability and compliance are critical. The goal is to verify that software operates correctly, safely, and effectively before release.

What are popular job titles related to Software Validation jobs in Minnesota? For Software Validation jobs in Minnesota, the most frequently searched job titles are:
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Software Validation jobs near you
Infographic showing various Software Validation job openings in Minnesota as of July 2026, with employment types broken down into 89% Full Time, 9% Part Time, and 2% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $114,712 per year, or $55.1 per hour.

Computer Systems Validation Engineer

Three Point Solutions, Inc.

Maple Grove, MN • On-site

Full-time

Re-posted 2 days ago

Job description

Job title : Computer Systems Validation Engineer-12345
Job Description:
About This Role:
  • To ensure the quality of our client's software applications and equipment by validating/qualifying to specifications.
  • Provide comprehensive documentation (specifications and validation/qualifications) per the division's policy to meet FDA regulations.

Your Responsibilities Include:
  • Define the development of comprehensive specifications (hardware and/or software) for equipment/software from basic functionality to complex systems such as PLC's, Visual Basic applications, databases, SCADA applications, and systems with FDA defined electronic records and electronic signatures.
  • Provide project estimates independently. Review estimates for Engineer I's.
  • Submit specification, protocol and report for approvals and documentation control via a Change Request.
  • Develop comprehensive software validations and/or equipment qualification protocols per the specification.
  • Execute software validation and/or qualification protocols & record results.
  • Document communicate and follow-up on software/equipment issues.
  • Complete project deliverables per project schedule and monitor project schedule and scope changes to assure team can meet delivery requirements.
  • Create documents, links and Change Requests utilizing a Product Data Management system.
  • Provide information on FDA/QSR regulations and internal process validation policy with regards to software validations, equipment installation qualifications, electronic records & signatures.
  • Develop and review comprehensive validation procedures in compliance with FDA.
  • Perform project lead activities on small to large-scale validation/qualification projects. Participate in vendor evaluations.
  • Provide guidance, mentoring and training to Engineer I's & II's. Ensure consistency of work among Engineer I's & II's. Provide peer reviews on specifications, protocols and reports.
  • Influences and defines functional, departmental and divisional policies & procedures through involvement with cross-functional engineering initiatives.
  • Provide leadership role on championing functional best practices.

What We're Looking For:
Minimum Qualifications:
  • Bachelor's Degree in Engineering Discipline
  • 5-9 years direct experience
  • Experience in Medical Device manufacturing specifically writing compliance documentation
  • In depth knowledge of MS Office tools
  • Must have excellent organization, clear verbal and written skills
  • Experience working in a SDLC-system development lifecycle
  • Hand on skills using navigating equipment user interfaces
  • High level attention to detail and ability to support multiple priorities at once
  • Must be team-oriented with people skills and positive can-do attitude in dealing with many customers, from various departments (Engineering, R&D, Manufacturing, Regulatory, etc.)

Preferred Qualifications:
  • Experience working in FDA-regulated industry
  • Experience working with a regulatory body in an audit
  • Performed in a quality role ensuring industry compliance
  • Practical knowledge of 21 CFR Part 11 (electronic records/electronic signature)

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