Senior Supplier Development Engineer
Job in
Irvine, Orange County, California, 92713, USA
Listed on 2026-02-21
Listing for:
Hydrogen Group
Full Time
position Listed on 2026-02-21
Job specializations:
-
Engineering
Quality Engineering, Manufacturing Engineer, Product Engineer, Process Engineer
Job Description & How to Apply Below
JOB TITLE: Senior Supplier Development Engineer
LOCATION: Irvine, CA (Onsite)
SCHEDULE: 8 AM - 5 PM
DURATION: 18-Month Contract
MAX PAY RATE: $54-59/hr
Job OverviewWe are seeking a Senior Supplier Development Engineer to join the Advanced (Use the "Apply for this Job" box below). Development Engineering team
. This role provides manufacturing engineering support for the design, development, and commercialization of implantable cardiovascular devices and delivery systems
. You will work with suppliers and cross‑functional teams to ensure design for manufacturability (DFM), supplier capability, and product quality from development through product launch.
- Provide technical input for strategic sourcing projects including supplier evaluation, part qualification plans, and specification reviews
- Participate in technical discussions with suppliers to improve products and processes
- Conduct design and drawing reviews to ensure manufacturability
- Define supplier qualification requirements for OEMs, contract manufacturers, and custom materials
- Lead supplier validations and support initial builds and commercialization of new product introductions
- Integrate new products into manufacturing, supporting phase‑in/phase‑out activities
- Manage product and supply chain readiness reviews and design transfers to manufacturing
- Respond quickly to supplier quality issues
, escalating as needed - Ensure Tier 1 suppliers are effectively using capable Tier 2 suppliers
- Align cross‑functional teams and suppliers on outstanding technical issues
- Work with suppliers to optimize processes
, reduce costs, and implement lean manufacturing principles - Develop and manage project milestones in line with product development and commercialization needs
- Perform supplier risk and capacity assessments and implement corrective actions
- Audit suppliers for technical capabilities and quality compliance
- Perform additional duties as assigned
- Bachelor's degree in Engineering or Scientific field with 4 years of experience
, or - Master's degree in Engineering or Scientific field with 3 years of experience
- Onsite work required
- Up to 20% domestic/international travel
- Experience with statistical tools (SPC, Six Sigma, DMAIC, etc.)
- Experience in catheter manufacturing technology for cardiovascular, endovascular, minimally invasive endoscopy, or implantable devices
- CAD experience (
ProE / Solid Works
) - Strong analytical, problem‑solving, and technical writing skills
- Strong project management skills
- Ability to work independently and collaboratively
- Excellent verbal, written, and interpersonal communication skills
, including conflict and relationship management
Position Requirements
10+ Years
work experience
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