Component Engineer

    Highlights

    Support an effort of the supply chain activity by identifying long lead time items and engaging with the suppliers for potential cross-references. Participate in DVT readiness and design reviews to identify component risks, manufacturability concerns, and documentation gaps.

    Numbers & Facts

    LocationIrvine, CA

    Description

    Responsibilities:
    • DVT & Design Release Support.
    • Participate in DVT readiness and design reviews to identify component risks, manufacturability concerns, and documentation gaps.
    • Support design transfer activities to ensure readiness for manufacturing release.
    • Component Risk & Lifecycle Assessment
    • Evaluate lifecycle status (NRND/EOL), supplier risk, and availability
    • Recommend alternates and mitigation strategies.
    • Support Release of OTS and custom parts
    • Mechanical Drawing Review & Manufacturability
    • Review drawings for dimensional accuracy, GD&T (ASME Y14.5), and tolerance stack-up risks.
    • Assess manufacturability relative to supplier capabilities.
    • Identify over-constrained tolerances and yield risks.
    • Provide actionable DFM/DFA feedback.
    • Cross-Functional Support
    • Act as liaison between Engineering and Supply Chain.
    • Support supplier technical discussions.
    • Assist in resolving build and early production issues.
    • Support an effort of the supply chain activity by identifying long lead time items and engaging with the suppliers for potential cross-references
    • Support lifecycle advancement of components in Propel by ensuring complete specifications, compliance, and approved sourcing for pre-production readiness.
    • Ensure alignment of component data across Propel/NetSuite.
    • Support traceability and audit readiness.

    Requirements:

    • Bachelor degree in Electrical, Mechanical Engineering, or related technical field.
    • 5+ years of experience in component engineering, hardware engineering, or a related technical role.
    • Experience supporting product development through DVT and design release phases.
    • Experience in a regulated environment (medical device preferred).
    • Hands-on experience working with cross-functional teams (Engineering, Supply Chain, Manufacturing)
    • Strong understanding of electronic, electromechanical, and mechanical components.
    • Experience evaluating component lifecycle (Active, NRND, EOL) and supply risk.
    • Ability to review datasheets and perform fit, form, and function analysis.
    • Ability to read and critically review mechanical drawings.
    • Working knowledge of GD&T (ASME Y14.5) principles.
    • Understanding of tolerance stack-up and its impact on assembly and performance.
    • Familiarity with common manufacturing processes (machining, molding, sheet metal) and associated constraints.
    • Familiarity with design transfer processes and production ramp considerations.
    • Familiarity with PLM systems (Propel) and ERP systems (NetSuite).
    • Understanding of ISO 13485 and FDA 21 CFR Part 820 requirements preferred.
    • Strong analytical and problem-solving skills with attention to detail.
    • Ability to identify risks and provide clear, actionable recommendations.
    • Effective communication across engineering and operations teams.
    • Ability to work independently in high-impact role with minimal supervision.
    • Strong organizational skills and ability to prioritize high value activities.

    Physical Demands:

    • Sitting at a desk utilizing a computer.

    Working Environment:

    • Typical office areas with offices, cubicles and conference rooms.

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