Senior Engineer, R&D

Posted 3 Days Ago
Be an Early Applicant
Irvine, CA, USA
In-Office
108K-153K Annually
Senior level
Healthtech • Pharmaceutical
The Role
Develops and validates medical device components and systems for transcatheter heart valve products. Leads FEA modeling, statistical shape modeling, bench and virtual test method development, clinically accurate model creation, and mechanical problem solving. Collaborates with clinical, manufacturing, quality, regulatory, and R&D teams while documenting results and supporting FDA and applicable standards compliance.
Summary Generated by Built In

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 R&D Engineering team, you will work closely with our Quality and Manufacturing teams to develop the latest tools 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:

This is an exceptional opportunity for an experienced medical device engineer who will apply knowledge of Finite Element Analysis (FEA), test method development for THV frames, access and delivery systems (DS) using bench and simulation modalities as part of a team to design and develop heart valve systems in support of company's strategic plan.


  • Collaborate with Clinical Development group to develop Statistical Shape Models for patient anatomy for implant, access and DS.
  • Collaborate with Clinical Development group and R&D group to develop boundary conditions.
  • Lead effort to develop FEA models for components and systems for access and DS products.
  • Support other FEA engineers in developing, modifying FEA for THV frames.
  • Lead effort to develop virtual and bench models like sample holders, clinically accurate compliant aortic roots, vessels, CAD and manufacturing (machining, molding).
  • Lead test method development for clinically accurate boundary conditions.
  • Collaborate with other groups to test non-metal components: tissue, polymer, fabric.
  • Challenge status quo to develop new test methods and/or procedures to increase speed of innovation and/or to reduce conservatism.
  • Provide support to sustaining function as needed.
  • Solve mechanical engineering problems at the component through system level.
  • Maintain accurate documentation of results and generate technical reports.
  • Maintain current knowledge of competitive technologies in addition to medical, technical, and biomedical developments related to company products and therapies.
  • Interface with R&D, manufacturing, clinical development, clinical affairs, quality and regulatory personnel to ensure compliance with internal and external policies and procedures, QSR, and FDA regulations.
  • Work closely with clinical development and/or physician partners in both a pre-clinical and clinical environment with strong knowledge and understanding of cardiovascular anatomy, structure of the heart, and valve diseases.

 

What you’ll need (Required):

  • Bachelor's Degree in Engineering or Scientific field, 4+ years’ experience - OR -
  • Master's Degree in Engineering or Scientific field, 3+ years’ experience

 

What else we look for (Preferred):

  • 2+ years of experience in the medical device industry
  • 6+ years of experience in simulation using FEA with commercially available software
  • A PhD in Engineering
  • In-depth knowledge of virtual simulation tools like ANSYS, ABAQUS etc.
  • Prior patient CT reconstruction experience using commercial software such as Materialise, Simpleware etc.Hands-on experience with bench fixture, model building.
  • Understanding of ISO, ASTM and other relevant standards for system testing.
  • Understanding of ASME V&V 40
  • Strong understanding of statistical techniques for data analysis and experience with statistical and programming software such as MATLAB, Minitab etc. is preferred.
  • Experience with non-linear materials like tissue, hyperelastic etc. is preferred.
  • Cardiovascular experience preferred.
  • Strong documentation skills; strong technical writing ability and good verbal communication skills.
  • Effective communication, listening, and diagnostic skills are required.
  • Prior experience with submissions to FDA and other regulatory bodies is helpful.
  • The ability to work well independently and as a team member is essential.

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 $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.


Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

Skills Required

  • Bachelor's degree in Engineering or a scientific field with 4+ years of experience
  • Master's degree in Engineering or a scientific field with 3+ years of experience
  • 2+ years of experience in the medical device industry
  • 6+ years of experience in simulation using commercially available FEA software
  • PhD in Engineering
  • In-depth knowledge of virtual simulation tools such as ANSYS or ABAQUS
  • Patient CT reconstruction experience using commercial software such as Materialise or Simpleware
  • Hands-on experience with bench fixtures and model building
  • Understanding of ISO, ASTM, and other relevant system testing standards
  • Understanding of ASME V&V 40
  • Statistical data analysis and experience with MATLAB, Minitab, or similar software
  • Experience with nonlinear materials such as tissue and hyperelastic materials
  • Cardiovascular experience
  • Strong documentation and technical writing skills
  • Strong verbal communication, listening, and diagnostic skills
  • Experience with FDA and other regulatory submissions
  • Ability to work independently and collaboratively

Edwards Lifesciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Edwards Lifesciences and has not been reviewed or approved by Edwards Lifesciences.

  • Healthcare Strength — Health coverage is considered strong, with multiple plan choices, HSA options, and fertility support, and the company highlights holistic well‑being programs.
  • Retirement Support — A company 401(k) match and well‑regarded retirement offerings add clear long‑term value to total compensation.
  • Equity Value & Accessibility — An Employee Stock Purchase Plan with a discount and look‑back feature makes equity ownership accessible and enhances the total rewards package.

Edwards Lifesciences Insights

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The Company
HQ: Irvine, CA
13,687 Employees
Year Founded: 1958

What We Do

Edwards Lifesciences (NYSE: EW), is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Our roots date back to 1958 when Miles Lowell Edwards, a retired engineer with a background in hydraulics and fuel pump operations, set out to build the first artificial heart. Edwards believed the heart could be mechanized and was encouraged by Dr. Albert Starr to focus on developing an artificial heart valve. After just two years, the first Starr-Edwards mitral valve was developed and successfully placed in a patient. This innovation spawned Edwards Laboratories. Miles’ fascination with healing the heart and helping patients with heart disease stemmed from his own experience with rheumatic fever as a teenager and continues to fuel our patient-first culture today. Today, we are as passionate about providing innovative solutions for people fighting cardiovascular disease as we have ever been. It's our Credo. It takes integrity, collaboration, innovation, and focus. We are leaders in the design and manufacture of tissue replacement heart valves and repair products as well as advanced hemodynamic monitoring. We partner with physicians to innovate products designed to help patients live longer, healthier, and more productive lives. Our work is both rewarding and a privilege. The importance of what we do defines our approach. We work together to create an environment where ideas can flourish and we provide our people with the resources, expertise and support to bring those ideas to life. For our legal terms and trademarks, please visit: https://www.edwards.com/legal/legal-terms

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