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Empower Computer System Validation Engineer Jobs

Supermicro

System Validation Engineer

San Jose, CA · On-site

$100K - $113K/yr

Supermicro Computer is currently looking for talented System Validation Engineer to partner with Hardware Designing team to validate in-house servers and workstation platforms, troubleshoot and ...

Lyte AI Inc.

System Validation Engineer

Sunnyvale, CA · On-site

... Engineering from a top research university * 3-6 years of hands‑on lab experience in PCB bringup, system validation, signal/power integrity, or failure analysis * Solid analog circuit knowledge ...

Apple

SerDes System Validation Engineer

Cupertino, CA · On-site

We are looking for a SerDes System Validation Engineer to lead system validation of mixed-signal SerDes IP. In this highly visible role, you will actively work within Analog-Mixed/Signal design team ...

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Empower Computer System Validation Engineer information

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How much do empower computer system validation engineer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for empower computer system validation engineer in the United States is $51.80, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $64.42 per hour, depending on experience, location, and employer.

What is the difference between Empower Computer System Validation Engineer vs Empower Computer System Validation Engineer?

AspectEmpower Computer System Validation EngineerEmpower Computer System Validation Engineer
CertificationsGxP, 21 CFR Part 11, CSV certificationsGxP, 21 CFR Part 11, CSV certifications
Work EnvironmentPharmaceutical, biotech, or medical device industriesPharmaceutical, biotech, or medical device industries
Employer UsageRegulated industries requiring validation of computer systemsRegulated industries requiring validation of computer systems

Both roles typically require similar certifications and work in regulated environments like pharmaceuticals and biotech. The primary difference lies in specific company or project terminology, but generally, they perform comparable validation tasks to ensure computer systems meet compliance standards.

What are popular job titles related to Empower Computer System Validation Engineer jobs?

For Empower Computer System Validation Engineer jobs, the most frequently searched job titles are:

Infographic showing various Empower Computer System Validation Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $107,747 per year, or $51.8 per hour.

Computer Systems Validation Engineer

Maple Grove, MN • On-site

Three Point Solutions, Inc.
Recruiting and Staffing Services • 11 - 50 employees
Learn more about Three Point Solutions, Inc.external

Contractor

Re-posted 10 days ago

Job description

Job Title: Computer Systems Validation Engineer
Client: Medical Device Manufacturing Company
Location: Maple Grove, MN 55311
Duration: 6 Months Contract
Focus Area: FDA-regulated Medical Device Software/Systems Validation
Position Overview
The Computer Systems Validation Engineer will be responsible for validating software and equipment in compliance with FDA regulations and company policies. This role will ensure that systems meet strict quality, compliance, and documentation standards. The ideal candidate will have strong technical expertise in validation processes, SDLC, and regulatory compliance, with experience in medical device manufacturing.
Key Responsibilities
  • Define, develop, and maintain comprehensive specifications for equipment/software (e.g., PLCs, Visual Basic apps, databases, SCADA applications, FDA-regulated systems).
  • Develop and review validation/qualification protocols, ensuring compliance with FDA requirements and QSR regulations.
  • Execute validation and qualification protocols, record results, and manage documentation via Change Requests.
  • Provide project estimates independently and review estimates for junior engineers.
  • Perform project lead activities on small to large-scale validation/qualification projects.
  • Ensure consistency and quality of validation work through peer reviews, mentoring, and training of Engineer I's and II's.
  • Support audits and regulatory inspections by providing accurate documentation and validation evidence.
  • Drive compliance with 21 CFR Part 11 (electronic records/e-signatures) and other FDA guidelines.
  • Influence cross-functional engineering initiatives and contribute to defining departmental best practices.

Required Qualifications
  • Bachelor's Degree in an Engineering discipline.
  • 5-9 years of direct experience in software/equipment validation within a regulated environment.
  • Strong background in medical device manufacturing and compliance documentation.
  • Hands-on experience with SDLC (System Development Life Cycle).
  • Excellent organizational, verbal, and written communication skills.
  • Proficiency in MS Office tools.
  • Ability to manage multiple priorities, with high attention to detail.
  • Strong interpersonal skills and a collaborative, team-oriented mindset.

Preferred Qualifications
  • Prior experience in an FDA-regulated industry.
  • Experience supporting audits and working with regulatory bodies.
  • Prior quality role experience ensuring compliance with industry standards.
  • Practical knowledge of 21 CFR Part 11 (electronic records/electronic signatures).

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