Component Engineer

Responsibilities

• 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.
• Mechanical Drawing Review & Manufacturability
• Review drawings for dimensional accuracy, GD&T (ASME Y14.5), and tolerance stack-up risks.
• Audit 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.
• Affiliate 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.
• 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.
• Familiarity with 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.