Edwards Lifesciences Corp

Senior Designer, UX

Edwards Lifesciences Corp$108K — $153K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in design, human-computer interaction, or related field + 5 years of relevant design experience.
  • Proficiency with Figma and usability tools like Dovetail or UserTesting.
  • Experience in planning and conducting usability testing following IEC 62366-1 standards.
  • Ability to communicate design rationale to senior stakeholders and drive function alignment.
  • Familiarity with regulatory expectations for Software as a Medical Device (SaMD) and quality management systems.

Responsibilities

  • Set the design direction and ensure quality consistency for a major product area.
  • Lead the development of design systems, including components and accessibility standards.
  • Oversee usability engineering activities, including usability testing and use-error analysis.
  • Collaborate with R&D, quality, regulatory, and clinical teams as a Human Factors Engineering contributor.
  • Influence product strategy alongside product management and engineering teams, mentoring designers across levels.

Benefits

  • Competitive salaries and performance-based incentives.
  • Diverse benefits programs catering to individual needs of employees and families.
  • Onsite role in Irvine, CA, fostering a collaborative work environment.
Full Job Description
At Edwards Lifesciences, the Implantable Heart Failure Management (IHFM) AI, Product and Platforms organization designs and builds the software and data products that clinicians and patients depend on. As a Lead Designer, you set the design direction for a product area and lead its design systems and usability engineering work. This is the entry level of the Subject Matter Expert (SME) track, where you combine deep design craft with technical and regulatory fluency. You are accountable for how IHFM products in your area look, feel, and perform for clinicians and patients, and for the software human factors evidence that supports their safe use.

How you'll make an impact
  • Set the design direction for a significant product area and ensure design quality and consistency across its features.
  • Lead design systems work for your area, owning components, patterns, accessibility standards, and contribution guidelines.
  • Lead usability engineering activities, including planning and overseeing formative and summative usability testing and use-error analysis that support regulatory submissions under IEC 62366-1.
  • Act as a Human Factors Engineering (HFE) contributor for Software as a Medical Device, partnering with research & development, quality, regulatory, and clinical stakeholders.
  • Influence product strategy alongside cross-functional marketing product management, technical product management, software engineering, and data engineering leadership, and mentor designers across levels.


What you'll need (Required):
  • Bachelor's degree in design, human-computer interaction, software human factors, or a related field plus five years of design experience, including leading the design of a major product area or equivalent work experience based on Edwards criteria
  • Deep proficiency with Figma and the team's research and usability toolset (e.g., Dovetail and / or UserTesting), design systems, and prototyping.
  • Experience planning and running formative and summative usability testing and applying software human factors methods.
  • This is an onsite role based in Irvine, CA. Relocation assistance is not provided, and candidates must reside within a 50-mile radius of Irvine to be considered.


What else we look for (Preferred):
  • The ability to communicate design rationale to senior stakeholders and to drive alignment across functions.
  • A track record of shipping high-quality design and improving outcomes through research and iteration.
  • Direct experience with usability engineering for medical devices (IEC 62366-1), including contributing to a usability engineering file or design history file.
  • Familiarity with SaMD regulatory expectations and quality management systems.
  • Experience owning a cross-product design system and accessibility framework.
  • Working knowledge of the technologies (Android, iOS, React, Angular, .NET Core, REST, Databricks, Snowflake) and interoperability standards (HL7, FHIR, IHE) sufficient to design within real technical constraints.


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 (CA), the base pay range for this position is $108,000 to $153,000 (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.

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

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