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Worksite Engineer Jobs (NOW HIRING)

The Validation Engineer II is a mid-level role responsible for creating, planning, and executing ... Maintains regular and consistent attendance at the primary worksite. * Other duties as assigned.

Process Engineer

Austin, TX · On-site

$60 - $95/hr

Chemical / Process Engineer - Advanced Manufacturing Location / Worksite On-site / Project-Based - Client Advanced Manufacturing Facility Specific project location to be confirmed. About Augment ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Human-Systems Integration (HSI), Task Analysis, Human Error Analysis, Worksite Analysis, Human-in ...

NY · On-site

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Human-Systems Integration (HSI), Task Analysis, Human Error Analysis, Worksite Analysis, Human-in ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Human-Systems Integration (HSI), Task Analysis, Human Error Analysis, Worksite Analysis, Human-in ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Human-Systems Integration (HSI), Task Analysis, Human Error Analysis, Worksite Analysis, Human-in ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Human-Systems Integration (HSI), Task Analysis, Human Error Analysis, Worksite Analysis, Human-in ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Human-Systems Integration (HSI), Task Analysis, Human Error Analysis, Worksite Analysis, Human-in ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Human-Systems Integration (HSI), Task Analysis, Human Error Analysis, Worksite Analysis, Human-in ...

As a Human Factors Engineer (HFE) within ACE, part of a small, passionate, and accomplished team of ... Human-Systems Integration (HSI), Task Analysis, Human Error Analysis, Worksite Analysis, Human-in ...

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Infographic showing various Worksite Engineer job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution.

Validation Engineer II

Carlsbad, CA

Alphatec Spine
Medical Equipment and Supplies Manufacturing • 501 - 1,000 employees

Full-time

Re-posted 2 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.