Staff Technologist, R&D TMTT

Reposted 7 Hours Ago
Be an Early Applicant
Irvine, CA, USA
In-Office
81K-114K Annually
Expert/Leader
Healthtech • Pharmaceutical
The Role
Provide hands-on engineering support for transcatheter valve delivery systems: design, fabricate, and test prototypes; develop test methods and protocols; perform measurements and failure analysis; document results; support manufacturing transfer and train staff while ensuring compliance with quality systems.
Summary Generated by Built In

At Edwards Lifesciences, patients are at the heart of everything we do. As a global leader in patient-focused medical innovations, we are dedicated to improving lives through breakthrough technologies. Our Research & Development teams work collaboratively to develop innovative products that address unmet patient needs and improve outcomes around the world.

 

Transcatheter Mitral and Tricuspid Therapies (TMTT) is dedicated to solving the complex challenges of mitral and tricuspid valve disease through breakthrough technologies that significantly improve patients' lives.

 

This role is part of the fast-paced, innovative EVOQUE program, a transcatheter tricuspid valve replacement technology. The position offers high visibility and hands-on technical support across multiple generations of delivery system development. This is an exciting opportunity for an experienced R&D professional to contribute to the design and development of next-generation structural heart therapies and help shape technologies that will transform patient care.

 

How You'll Make an Impact

  • Serve as a subject matter expert (SME) providing broad engineering support across testing, checkout, modification, fabrication, and assembly activities while identifying opportunities for technical improvements and solutions.

  • Partner closely with R&D engineers throughout the design and development process.

  • Brainstorm, evaluate, and translate concepts into new product designs.

  • Apply mechanical engineering principles to delivery systems, implants, and accessory device development.

  • Design, build, and fabricate complex prototypes, sub-assemblies, fixtures, and tooling.

  • Utilize rapid prototyping techniques for metal and plastic components.

  • Build prototypes for feasibility testing and physician demonstrations.

  • Recommend materials and manufacturing approaches for prototypes and product designs.

  • Perform feasibility, operational, design verification, animal, and cadaver testing.

  • Develop, validate, and execute test methods, protocols, and procedures.

  • Characterize device performance against design requirements and specifications.

  • Identify failure modes, perform root cause analysis, and implement corrective solutions.

  • Collect, document, analyze, and communicate test data and results.

  • Perform precision measurement and testing utilizing calipers, micrometers, microscopes, optical systems, tensile testers, and inspection fixtures.

  • Operate, set up, maintain, and support calibration of laboratory equipment.

  • Create and maintain design documentation, drawings, test reports, procedures, and engineering records in accordance with quality system requirements.

  • Apply Design for Manufacturing (DFM) and Design for Automation (DFA) principles during development activities.

  • Support manufacturing and operations through process development, tooling support, troubleshooting, and training.

  • Train and mentor assemblers, contractors, and junior employees.

  • Collaborate cross-functionally with R&D, Manufacturing, and Quality teams to ensure compliance with internal procedures and protocols.

  • Read, interpret, create, and modify CAD models and technical drawings.

  • Maintain compliance with quality systems, laboratory procedures, and safety requirements.

  • Independently solve complex technical and engineering challenges.

  • Perform general laboratory support activities, equipment maintenance, and organizational tasks as needed.

 

What You'll Need (Required Qualifications)

  • High School Diploma, technical certification, or equivalent experience and:

    • 13 years of experience in an R&D laboratory, engineering development, or medical device environment; OR

    • 15 years of directly related technical experience

 

What Else We Look For (Preferred Qualifications)

  • Experience with machining operations including milling, turning, grinding, polishing, and related fabrication processes is highly preferred

  • Medical device experience supporting structural heart, transcatheter, catheter-based, or implantable technologies is highly preferred

  • Proven catheter and implant prototyping and product development experience is highly preferred

  • Experience performing device, component, material, or system testing.

  • Strong mechanical aptitude and ability to independently solve complex technical problems.

  • Experience with extrusion, laser cutting, laser welding, fluoropolymer processing, thermoplastics, thermosets, and Nitinol (NiTi) processing.

  • Ability to design and fabricate precise tooling utilizing metal and plastic materials.

  • Experience operating and maintaining additive manufacturing equipment and 3D printing technologies.

  • Demonstrated ability to create novel device concepts and platforms from the ground up.

  • Proficiency with SolidWorks and Creo/ProE CAD software.

  • Ability to work independently with minimal supervision in a fast-paced development environment.

  • Strong communication, documentation, and organizational skills.

  • Medical device experience supporting structural heart, transcatheter, catheter-based, or implantable technologies is a huge plus

  • Knowledge of medical device design controls, quality systems, and engineering change processes.

  • Experience managing project expenses, purchase orders, and invoice approvals.

  • Demonstrated ability to work effectively across multidisciplinary teams.

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 $81,000 to $114,000 (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

  • High School Diploma, technical certification, or equivalent experience
  • 13 years of experience in an R&D laboratory, engineering development, or medical device environment OR 15 years of directly related technical experience

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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