Component Engineer

Katalyst Healthcares and Life Sciences

Irvine, CA

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.

Apply

Vacancy posted 3 days ago

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