Senior Engineer, R&D Testing

Posted 8 Hours Ago
Be an Early Applicant
Irvine, CA, USA
In-Office
108K-153K Annually
Senior level
Healthtech • Pharmaceutical
The Role
Lead development and qualification of test systems, methods, and analytics to evaluate medical device performance. Design and run experiments, analyze data, author reports, create design control documentation, manage supplier criteria, plan engineering projects, and mentor technicians while collaborating with Quality and Manufacturing.
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.

Dedicated to innovation, our Surgical business unit is focused on identifying and solving critical, unmet needs in cardiac surgery. In understanding the challenges of open-heart surgery, we partner with surgical teams to deliver modern technologies intended to enhance patients’ quality of life and expand their potential treatment opportunities. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. The Senior Engineer applies knowledge of technical principles and Edwards systems/procedures to optimize product development.
How you’ll make an impact:

  • Innovate, develop, and qualify new test systems, test methods, SOPs, R&D processes, analytics routines, engineering models, etc., to evaluate product performance.

  • Create, evaluate, and improve on products by developing designs, leading experiments (including writing and executing protocols), analyzing results, making recommendations, and authoring reports, based on strong engineering principles.

  • Create/update complex design control documents including requirement specs and risk documents.

  • Develop and execute engineering project plans.

  • Identify, evaluate, manage, and provide guidance to suppliers, including establishing tolerances and defining acceptance criteria for suppliers.

  • Assign R&D support tasks, give instruction to technicians on conducting tests, train technicians and provide feedback, coordinate technician work.

  • Evaluate input and form technical recommendations including designing test systems and processes, parts, components and subsystems.

  • Train, coach, and guide lower level employees on routine procedures.

  • Other duties assigned by leadership.

What you'll need (Required):

  • Bachelor's Degree in Engineering or Scientific field, 4 years experience, OR

  • Master's Degree or equivalent in Engineering or Scientific field, 3 years experience, OR

  • Ph.D. or equivalent in Engineering or Scientific field

What else we look for (Preferred):

  • Strong background with test method development and qualification, experimental design, product testing, data analysis, and test lab equipment.

  • Strong background and knowledge of engineering principles, theories, and concepts (special consideration will be given for prior experience with experimental fluid mechanics and/or heart valve performance).

  • Proficiency with CAD and fabrication, statistical techniques and software.

  • Basic proficiency with AI, automation, programming, and/or medical image analysis is desired.

  • Basic familiarity with systems engineering, predictive engineering, and reliability concepts is desired.

  • Medical device industry exposure is strongly desired.

  • Strong problem-solving, organizational, analytical and critical thinking skills.

  • Strong documentation, communication (e.g., written and verbal) and interpersonal relationship skills including consultative and relationship management skills.

  • Demonstrated ability to influence change, thrive in complex teams, and represent the team professionally on broad projects.

  • Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations.

  • Ability to manage competing priorities in a fast-paced environment.

  • Proficiency with MS Office is required.

  • 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 $108,000 - $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.

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.

Skills Required

  • Bachelor's Degree in Engineering or Scientific field plus 4 years experience OR Master's Degree plus 3 years experience OR Ph.D. in Engineering or Scientific field
  • Proficiency with MS Office
  • Experience with test method development, experimental design, product testing, and test lab equipment
  • Knowledge of engineering principles; experience with experimental fluid mechanics and/or heart valve performance
  • Proficiency with CAD and fabrication
  • Familiarity with statistical techniques and software
  • Basic proficiency with AI, automation, programming, or medical image analysis
  • Familiarity with systems engineering, predictive engineering, and reliability concepts
  • Medical device industry experience
  • Strong documentation, communication, and interpersonal skills

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.

  • Retirement Support Retirement programs include a 401(k) match complemented by a separate profit‑sharing contribution. These elements add meaningful long‑term value to total compensation.
  • Equity Value & Accessibility An employee stock purchase plan with a discount and look‑back feature, alongside stock awards for eligible roles, provides notable upside. Program expansions indicate continued accessibility.
  • Leave & Time Off Breadth Time‑off policies include generous PTO, company holidays, and a year‑end holiday shutdown. These offerings enhance work‑life support when available at the site.

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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