Component Engineer

Component Engineer

Location:

Irvine, CA (Onsite)

Duration: 12+ months

• 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.
• Evaluate lifecycle status (NRND/EOL), supplier risk, and availability; recommend alternates and mitigation strategies.
• Support release of OTS and custom parts.
• Review mechanical 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.
• Act as liaison between Engineering and Supply Chain; support supplier technical discussions; assist in resolving build and early production issues; identify long lead time items and engage suppliers for potential cross-references.
• Support lifecycle advancement of components in Propel ensuring complete specifications, compliance, and approved sourcing for pre-production readiness; ensure alignment of component data across Propel/Net Suite; support traceability and audit readiness.

• 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 (Net Suite).
• 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.

Sitting at a desk utilizing a computer

Typical office areas with offices, cubicles and conference rooms.