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Director, Supplier Development Engineering
Job in
Irvine, Orange County, California, 92713, USA
Listed on 2026-01-15
Listing for:
Edwards Lifesciences
Full Time
position Listed on 2026-01-15
Job specializations:
-
Engineering
Product Engineer, Biomedical Engineer
Job Description & How to Apply Below
Join to apply for the Director, Supplier Development Engineering role at Edwards Lifesciences
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Innovation starts from the heart. Edwards Lifesciences is a leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Director of R&D Supplier Development Engineering is a unique career opportunity that could be your next step toward an exciting future.
Impact- Partner with R&D leaders in the design and development of the delivery system products and be accountable for achieving new and generational improvements of this transcatheter replacement therapy.
- Hands‑on leader with sound technical knowledge, strong leadership skills, and the ability to guide and develop a highly driven and technical team.
- Lead the team responsible for design and development with suppliers, development and testing of complex interventional catheters for delivery of implantable devices with suppliers.
- Demonstrate focus on staff development, ethics, and motivation through appropriate assignment of opportunities and training activities to support the achievement of both professional development goals and business goals.
- Actively engage in development of staff performance management objectives (PMOs), ensuring deliverables are met on time.
- Manage and drive timelines for feasibility testing activities, design verification testing, clinical trials and supplier validations for commercial release testing.
- Build and maintain strong relationships with R&D, Suppliers, Program Management, Manufacturing, and Supplier Quality to ensure successful project execution and compliance with internal policies and procedures (QSR, FDA Regulations, and ISO Standards).
- Partner and support product development efforts in the design and iteration of new delivery systems, and components for transcatheter tricuspid valve replacement technologies.
- Bachelor's degree in a related field (Engineering, Applied Sciences, etc.) and experience in engineering.
- Demonstrated track record in management of technical and/or engineering disciplines.
- Master's degree or PhD in engineering (Mechanical or Biomedical).
- Medical device experience in new product development with successful design optimization from development to commercialization.
- Experience managing engineering teams and cross‑functional relationships.
- Experience managing external vendors.
- Experience with rapid product development in cross‑functional teams, creative design, prototyping, and test method development (in‑vitro testing).
- Proven ability to apply technical knowledge and judgment to complex engineering problems. Knowledge of DFM, GD&T and Six Sigma methodology.
- Skills in biomechanical design and delivery system catheter design.
- Experience in catheter and related manufacturing (extrusions, braiding, molding, laser‑cutting and bonding processes).
- Strong interpersonal and people management skills. High emotional intelligence.
- Displays broad perspective and effective judgment, demonstrates well‑reasoned problem solving and decision‑making. Ability to be bold and decisive to drive action.
- Builds a shared vision; inspires others to action; sets clear direction; establishes plans consistent with that direction.
- Demonstrates a sense of urgency; understands the importance of outperforming and outpacing the competition in meeting customer and patient needs.
- Ability to work in a matrix organization and lead cross‑functional teams.
- Able to demonstrate strong skills as an innovator, problem solver, and mentor.
- Strong problem solving and root cause analysis skillset and the ability to rapidly iterate and react to clinical device feedback.
- Preferred background includes experience in more than one of the following areas:
Interventional access devices, rapid product development, and manufacturing of components and complex assembly design.
Aligning our overall business objectives with performance, we offer competitive salaries, performance‑based incentives, and a wide…
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