Senior Principal Engineer, Supplier Development

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profile Job Location:

Irvine, CA - USA

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Imagine how your ideas and expertise can change a patients life. Our Global Operations & Quality team plays a central part in ensuring our products are delivered to patients with cardiovascular disease. Youll partner cross-functionally with manufacturing operations and sales teams delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. Whether your work includes strategic inventory planning labeling warehouse management material handling or any of our other supply chain opportunities you will be making a meaningful contribution to our team and to patients all over the world.

The Senior Principal Engineer will serve as a key technical subject matter expert partnering closely with internal teams and external suppliers to ensure product designs meet user needsincluding ease of use manufacturability cost effectiveness and operational addition to deep technical leadership this role requires strong project management capabilities and a thorough understanding of Design Control and Catalyst processes to drive effective compliant and timely project execution.

How youll make an impact:

  • Build and maintain strong partnerships with R&D Program Management Manufacturing Supplier Quality and key suppliers to ensure seamless project execution and compliance with internal procedures QSR FDA regulations and ISO standards.

  • Support and contribute to product development efforts by influencing the design and iteration of nextgeneration delivery systems and components for Advanced Technologies and Surgical Therapies.

  • Serve as a handson technical leader with strong engineering expertise and the ability to coach mentor and elevate a highperforming technically skilled team.

  • Lead crossfunctional teams and external suppliers in the design development and testing of complex interventional catheter delivery systems for implantable devices.

  • Champion team development ethics and engagement by providing meaningful growth opportunities targeted training and clear guidance to support both professional and business objectives.

  • Oversee and drive timelines for feasibility studies design verification testing clinical evaluations and supplier validation activities required for commercial release.

  • Perform other duties and responsibilities as assigned.

What we look for:

  • Bachelors degree in engineering or scientific with 8 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:

  • Masters degree in engineering and/or MBA.

  • 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.

  • Technical skills in biomedical design and delivery system catheter design.

  • Proven ability to manage and collaborate with external vendors to meet quality timeline and technical requirements.

  • Strong experience in rapid product development within crossfunctional teams including creative design iteration prototyping and test method development (e.g. invitro testing).

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 $139000 - $196000 (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.


Required Experience:

Staff IC

Imagine how your ideas and expertise can change a patients life. Our Global Operations & Quality team plays a central part in ensuring our products are delivered to patients with cardiovascular disease. Youll partner cross-functionally with manufacturing operations and sales teams delivering thought...
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Key Skills

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About Company

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Edwards Lifesciences (NYSE: EW), is the global leader of patient-focused medical innovations for structural heart disease and critical care monitoring. We are driven by a passion for patients, dedicated to improving and enhancing lives through partnerships with clinicians and stakehol ... View more

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