- Irvine, California, United States
- On-site
- Full-time · Senior
- $121K–$171K per year
- 6+ years
Technical subject matter expert role for Surgical Therapies focusing on supplier validation, product development, and design control for cardiovascular medical devices.
Compensation
For California, the base pay range for this position is $121,000 - $171,000 (highly experienced).
Responsibilities
- Lead the end-to-end technical validation of suppliers during product development, from component design and GD&T reviews to process characterization, capability analysis, and strategic process validation
- Build and maintain strong partnerships with R&D, Program Management, Manufacturing, Supplier Quality, and key suppliers
- Support and contribute to product development efforts by influencing the design and iteration of next-generation delivery systems and components
- Lead cross-functional teams and external suppliers in the design, development, and testing of complex interventional catheter delivery systems
- Oversee and drive timelines for feasibility studies, design verification testing, clinical evaluations, and supplier validation activities
Requirements
- Bachelor's degree in engineering or scientific
- Master’s degree in engineering and/or MBA
- Nice to have: Interventional access devices
- Nice to have: Rapid product development
- Nice to have: Component-level manufacturing