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Job Details

Designer, Engineering

Type

Full time

Location
USA - California – Irvine
Job reference

Req-39080

Posted for

1 day ago

Innovation starts from the heart. At Edwards, we put patients first. We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structural heart disease. As part of our New Product Development Engineering team, you will work closely with our R&D, Pilot Manufacturing, and Quality teams to develop the latest products and technologies to address significant, unmet clinical needs that impact patients’ lives around the world.

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.

How you will make an impact:

  • Creating new designs utilizing parametric solid modeling software or applications to develop basic data, assemblies and detailed parts of devices, mechanisms, and structures, assess viability of engineering specifications/concepts including advising engineers on suggested revisions on designs.
  • Designing complex tooling fixtures, incorporating ease of manufacturing, safety, performance, and reliability; and selecting equipment and materials, contractual specification requirements and cost; including recommending alternates and solutions needed to achieve the intended design objective. Identifying design errors, omissions, and other deficiencies, and recommending revisions and/or improvements in design layout to responsible engineers or designers throughout the validation process including redline reviews.
  • Process Engineering Change Requests (ECR) including describing changes and providing corresponding technical justification; checking completed layouts and drawings for clarity, completeness, conformity to standards, procedures, specifications; and accuracy of calculations and dimensioning and notes necessary to present design proposals.
  • Consulting with and providing input to Engineers on Edwards drawing standards and CAD tools, maintaining integrity of the CAD PDM (Product Data Management) modeling software.
  • Developing presentations and presenting proposal on designs across internal and external functions to secure consensus on the design viability and functionality.

What you’ll need (Required):

  • H.S. Diploma or equivalent with 8 years of previously related experience Required.

What else we look for (Preferred):

  • Associate’s Degree or equivalent in related field preferred
  • Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills
  • Problem solving methodology, tolerance analysis, and GDP (Good Documentation Practices)
  • Proven expertise in usage of CAD (e.g. Creo, Solidworks, AutoCAD, CAD PDM) and MS Office Suite
  • Experience reading, interpreting, and creating drawings
  • Ability to read, comprehend, write, and speak English
  • Full understanding of CAD design principles, techniques and procedures including parametric solid models
  • Full understanding of ASME Y14.5M-1994 drawing standards
  • Advanced ability to utilize 2-D and 3-D CAD software
  • Good understanding of fabrication processes (e.g. machining, molding) to leverage in creating and evaluating designs
  • Full understanding of materials and materials properties
  • Good understanding of DFM (Design for Manufacturing) concepts and principles
  • Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines
  • Strict attention to detail
  • Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific projects
  • Ability to build productive internal/external working relationships

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 $72,000 to $102,000 (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.   

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Job reference

Req-39080

Jetzt Bewerben
Type

Full time

Location
USA - California – Irvine
Posted for

1 day ago


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About Edwards Lifesciences

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.


Wichtiger Hinweis für Kandidaten

COVID-Impfvorschrift

Edwards hat sich verpflichtet, die Anforderungen und Richtlinien unserer Regierungsbehörden einzuhalten und unsere gefährdeten Patienten und die Gesundheitsdienstleister, die sie auf der ganzen Welt behandeln, zu schützen. Aus diesem Grund ist für alle Positionen im Gesundheitswesen eine COVID-19-Impfung erforderlich, d. h. für alle, die direkt mit Patienten zu tun haben, und für alle, die im Rahmen ihrer Tätigkeit mit Gesundheitsdienstleistern zu tun haben. Wenn Sie eingestellt werden, müssen Sie als Einstellungsvoraussetzung nachweisen, dass Sie vollständig gegen COVID-19 geimpft sind oder eine gültige religiöse oder medizinische Befreiung von der Impfung haben. Diese Impfpflicht gilt nicht in Ländern, in denen es gesetzlich verboten ist, eine Impfung vorzuschreiben. In Ländern, in denen weniger Impfstoffe zur Verfügung stehen oder andere Anforderungen bestehen, können wir alternative Maßnahmen ergreifen, die die Sicherheit der Patienten und des medizinischen Personals optimieren, z. B. regelmäßige COVID-Tests oder spezielle Maskierungsanforderungen.

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