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Boeing Software Verification Validation Engineer Jobs

Alphatec Spine

Validation Engineer II

Carlsbad, CA · On-site

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes.

Abbott

Software Verification Engineer III

Little Canada, MN · On-site

$100 - $125/hr

Title: Software Verification Engineer III Location: St. Paul, MN Duration: 7 Months 100% Onsite ... Strong interest in product verification, validation, testing, and quality. * Ability to develop and ...

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How much do boeing software verification validation engineer jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for boeing software verification validation engineer in the United States is $56.31, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $70.43 per hour, depending on experience, location, and employer.

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Validation Engineer II

Carlsbad, CA • On-site

Alphatec Spine
Medical Equipment and Supplies Manufacturing • 501 - 1,000 employees
Learn more about Alphatec Spineexternal

Full-time

Re-posted 26 days ago

Job description

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing software verification activities, and contributing to continuous improvement and validation processes. The Validation Engineer II operates under limited supervision and collaborates closely with R&D, Software Engineering, Quality Engineering, Mechanical Engineering, Marketing, and Regulatory to deliver innovative products to market in accordance with FDA, ISO, and IEC standards.

The Validation Engineer II supports a broad range of software-enabled medical devices within a product suite that includes intraoperative neuromonitoring, surgical alignment, robotic navigation, and a cloud-based end-to-end platform, among others.

The ideal candidate has experience validating software-based medical devices as well as strong technical, troubleshooting, documentation, and communication skills, and the ability to work seamlessly with cross-functional teams.

Essential Duties and Responsibilities

  • Leads verification and validation activities for assigned projects, ensuring quality, timeline, and compliance expectations are met while working alongside cross-functional teams.
  • Defines verification strategies for new product development, authoring high-quality test plans and protocols.
  • Supports continuous improvement of V&V practices by identifying inefficiencies, implementing process improvements, and participating in cross-functional problem-solving.
  • Creates and reviews design control documentation, ensuring requirements, test plans and protocols, test reports, and traceability meet FDA and internal quality standards.
  • Designs, develops, and qualifies manual and automated system-level test methods.
  • Performs validation of non-medical-device software tools and supporting systems as required, ensuring appropriate rigor and documentation.
  • Supports risk management activities in accordance with ISO 14971 by contributing to hazard analysis, risk controls, and verification of risk mitigations.
  • Seeks guidance from and collaborates with senior validation engineers; may informally assist with onboarding or knowledge sharing for newer team members.
  • Maintains regular and consistent attendance at the primary worksite.
  • Other duties as assigned.

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