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Senior Mechanical Design Engineer-- KAUDC

Job in Irvine, Orange County, California, 92713, USA
Listing for: Compunnel Inc.
Seasonal/Temporary position
Listed on 2026-01-12
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 60 - 62 USD Hourly USD 60.00 62.00 HOUR
Job Description & How to Apply Below
Position: Senior Mechanical Design Engineer-- KAUDC5698409

Senior Mechanical Design Engineer – KAUDC
5698409

Base pay range: $60.00/hr – $62.00/hr

JOB SUMMARY

The Senior Supplier Development Engineer will provide manufacturing engineering support in the design and development of implantable devices and delivery systems to treat cardiovascular disease. This role spans from early product development through commercialization, ensuring supplier capability, manufacturability, and compliance with quality standards. The engineer will lead supplier validation activities, manage design transfers, and collaborate with suppliers and cross‑functional teams to optimize processes and support new product introduction.

KEY RESPONSIBILITIES
  • Provide technical input for strategic sourcing projects, including supplier capability evaluation, part qualification, specification review, and product implementation
  • Participate in technical discussions with suppliers to identify and implement product/process improvements
  • Conduct design and drawing reviews to ensure manufacturability
  • Define supplier qualification requirements for OEMs, contract manufacturers, and custom materials
  • Lead supplier validations and inspection fixture design for test method validation
  • Respond urgently to quality issues and escalate appropriately
  • Ensure Tier 1 suppliers use capable Tier 2 suppliers; resolve inter-company conflicts
  • Align cross‑functional teams and suppliers on outstanding issues
  • Work with suppliers to optimize processes, reduce costs, and implement lean manufacturing
  • Develop and manage project milestones for development and commercialization
  • Perform supplier risk and capacity assessments; take corrective actions
  • Audit suppliers for technical and quality capabilities
  • Support manufacturing readiness and supply chain readiness reviews
  • Manage product phase‑in/phase‑out activities around design, regulatory, and clinical requirements
MANDATORY QUALIFICATIONS (Must‑Have Skills)
  • Bachelor’s degree in Engineering or Scientific field with 4+ years of experience OR Master’s degree with 3+ years of experience
  • On‑site work availability
  • Ability to travel up to 20% (domestic/international)
  • Strong analytical, problem‑solving, and technical writing skills
  • Effective verbal/written communication and interpersonal skills, including conflict and relationship management
  • Ability to work independently and as part of a team
GOOD‑TO‑HAVE QUALIFICATIONS (Preferred Skills)
  • Experience with statistical tools (SPC, Six Sigma, DMAIC)
  • Experience in catheter manufacturing technology (cardiovascular/endovascular devices, minimally invasive endoscopy, implantable devices)
  • CAD experience (ProE/Solid Works)
  • Experience in supplier audits and validations
  • Familiarity with lean manufacturing and waste reduction practices

Seniority level:
Mid‑Senior level

Employment type:

Contract

Job function:
Medical Equipment Manufacturing and Medical Practices

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Position Requirements
10+ Years work experience
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