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Senior Supplier Development Engineer; Implantable Medical Devices KAUDC

Job in Irvine, Orange County, California, 92713, USA
Listing for: Compunnel Inc.
Full Time position
Listed on 2025-12-27
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Product Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 60 - 65 USD Hourly USD 60.00 65.00 HOUR
Job Description & How to Apply Below
Position: Senior Supplier Development Engineer (Implantable Medical Devices)-- KAUDC5698409

Senior Supplier Development Engineer (Implantable Medical Devices) – KAUDC
5698409

1 day ago – Be among the first 25 applicants.

This range is provided by Compunnel Inc. Your actual pay will be based on your skills and experience—talk with your recruiter to learn more.

Base pay range

$60.00/hr – $65.00/hr

Direct message the job poster from Compunnel Inc.

Responsibilities
  • Our Senior Supplier Development Engineer position is a unique career opportunity that could be your next step towards an exciting future. The Senior Supplier Development Engineer role will reside in the Advanced (Use the "Apply for this Job" box below). Development Engineering team to provide manufacturing engineering support in the design and development of implantable devices and delivery systems to treat cardiovascular disease.
  • Conduct engineering activities from initial product development phase through product launch. Develop manufacturing technologies to meet new product demands.
  • Apply Design for Manufacturability (DFM) concepts, tools and analysis. Conduct reviews to ensure DFM considerations are incorporated into designs.
  • Assess and develop supplier part capability. Work directly with suppliers to address specifications and quality requirements.
  • Lead supplier validation activities, support initial builds and commercialization of new product introduction. Integrate new products into manufacturing.
  • Manage product phase in/phase out activities around design, regulatory and clinical requirements.
  • Support manufacturing readiness reviews, supply chain readiness review and manage design transfers to manufacturing.
How you’ll make an impact
  • Provide technical input for strategic sourcing projects, including evaluation of supplier capability, part qualification plan, specification review, product implementation and part transition to manufacturing.
  • Participate in technical discussions with suppliers to identify and implement improvements in products and processes.
  • Perform design and drawing reviews to ensure that components meet desired capabilities for manufacturing.
  • Responsible for defining supplier qualification requirements for OEM, Contract manufacturer (components and devices) and custom materials, including supplier validations and Client receiving inspection fixture design for Test method validation.
  • Respond with a high sense of urgency to quality issues and elevate/communicate appropriately.
  • Ensure that Tier 1 suppliers are using capable Tier 2 suppliers and resolve any inter-company conflict effectively. Strategically bring various cross‑functional teams and suppliers in alignment on outstanding issues in a timely manner.
  • Work with suppliers to optimize processes, reduce cost, ensure lean manufacturing and remove waste from processes.
  • Develop and manage project milestones in line with development and commercialization needs.
  • Perform supplier risk & capacity assessment and take appropriate actions to ensure timely and successful commercialization. Audit suppliers for their technical capabilities as well as quality criteria.
  • Perform other duties and responsibilities as assigned.
Required Qualifications
  • Bachelor's Degree or equivalent in Engineering or Scientific field with, 4 years’ experience including either industry or industry/education OR Master's Degree or equivalent in Engineering or Scientific field with, 3 years’ experience including either industry or industry/education.
  • Up to 20% domestic/international travel required.
Preferred Qualifications
  • Experience in the use of statistical tools required (SPC, Six Sigma, DMAIC, etc.).
  • Experience in catheter manufacturing technology in the development of cardiovascular and/or endovascular devices, minimally invasive endoscopy and implantable devices.
  • CAD experience using ProE/Solid Works.
  • Strong analytical, problem solving and technical writing skills.
  • Ability to work well both independently and as a member of a team.
  • Effective verbal/written communication and interpersonal skills including conflict and relationship management.
Seniority level

Mid‑Senior level

Employment type

Contract

Industries

Medical Practices and Medical Equipment Manufacturing

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Position Requirements
10+ Years work experience
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