Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards’ groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
The Engineer II, Supplier Development will be part of the Transcatheter Heart Valve (THV) Supplier Development Engineering team, providing manufacturing engineering leadership to support the design, development, and commercialization of implantable devices and catheter‑based delivery systems for the treatment of cardiovascular disease.
How you’ll make an impact:
- Support strategic sourcing initiatives, including supplier capability assessments, part qualification strategies, specification reviews, and transition of products into manufacturing.
- Develop and mature manufacturing technologies and processes to support new product requirements and scale‑up needs.
- Support manufacturing readiness reviews (MRR) and supply chain readiness reviews (SCR), and lead robust design transfer activities into the production environment.
- Manage product phase‑in and phase‑out activities, ensuring alignment with design, regulatory, clinical, and manufacturing requirements.
- Support supplier validation activities and support milestone builds, NPI commercialization, and seamless integration of new products into manufacturing operations.
- Optimize Design for Manufacturability (DFM) by conducting design, drawing, and specification reviews to ensure components meet manufacturing capability and quality expectations.
- Assess, develop, and continuously improve supplier part and process capability through data‑driven evaluations and technical collaboration.
- Actively engage suppliers in technical discussions to identify and implement product and process improvements that enhance quality, reliability, and cost effectiveness.
- Define and execute supplier qualification and validation requirements for OEMs, contract manufacturers (component and device level), and custom material suppliers.
- Ensure Tier 1 suppliers effectively manage and qualify Tier 2 suppliers, resolving inter‑company issues to protect product quality and supply continuity.
- Align cross‑functional teams (R&D, Quality, Operations, Supply Chain, Regulatory) and suppliers to resolve open issues and meet program timelines.
- Partner with suppliers to optimize manufacturing processes, reduce cost, support lean manufacturing initiatives, and eliminate waste.
- Perform supplier risk, capacity, and continuity assessments, and drive mitigation plans to ensure successful on time commercialization.
- Audit supplier technical capabilities and quality systems to ensure compliance with performance, regulatory, and quality requirements.
What you’ll need (Required):
- Bachelor's degree in engineering or scientific, with 2 years of experience in new product development, process development, commercialization, and/or operations engineering in a medical device industry.
- Travel up to 25% domestically and internationally.
- On-site work required.
What else we look for (Preferred):
- Experience in medical device new product development, including successful design optimization and progression from early development through commercialization.
- Background in at least two of the following areas: interventional access devices, rapid product development, component-level manufacturing, or complex assembly design.
- Hands-on experience with catheter manufacturing processes, such as extrusions, braiding, molding, laser welding, and bonding techniques.
- Demonstrated capability to apply sound engineering judgment and technical expertise to solve complex problems; working knowledge of DFM, GD&T, and Six Sigma methodologies.
- Experience in rapid product development within cross‑functional teams, including creative design iteration, prototyping, and test method development (e.g., in‑vitro testing).
- Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California, the base pay range for this position is $87,000 - $123,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
COVID Vaccination Requirement
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.