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Salary
≈ $44k – $109k per year (Estimated)
Location
In office (Caesarea)
Seniority
Junior · 2+ years exp
Visa
Sponsors visas in United States, Ireland, United Kingdom; no register of this country names it
Employment
Contractor

Confirmed on the employer's own hiring board on Nov 11, 2026. First seen by Alion on Sep 22, 2026. Edwards Lifesciences scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Edwards Lifesciences is an American medical device company that became independent from Baxter in 2000 but traces its work to the first commercially available artificial heart valve, developed by Miles Lowell Edwards in the late 1950s. It concentrates entirely on structural heart disease and critical care monitoring, and its transcatheter aortic valve replacement business changed cardiac practice by allowing valves to be delivered through a catheter rather than through open chest surgery. Headquartered in Irvine, California and listed on the New York Stock Exchange, it holds a leading position in a market it largely created.

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.

Our Advanced Technology (AT) teams harness the imagination, courage, and resourcefulness to think beyond what’s currently possible, and create solutions for patients many years into the future. If you’re an early-stage innovator, then Edwards AT team is the place for you to take the next steps in your career. We’ll give you the tools and resources you need to create groundbreaking innovations that shape the future of structural heart technology

How you will make an impact:

  • Design, execute, and support a variety of testing platforms, including benchtop setups, ex-vivo experiments, and in-vivo studies
  • Collaborate with cross-functional teams, including mechanical engineers and physician to define and refine product design requirements through iterative development process
  • Support pre-clinical studies preparation, execution, documentation, and post-study analysis in collaboration with internal and external partners.
  • Develop test methods, protocols, and experimental setups to evaluate product performance and design concepts.
  • Take part in prototype development, characterization, and validation activities.
  • Analyze testing results and translate data into actionable design insights
  • Drive hands-on experimental work to enable rapid learning cycles and informed design decisions.
  • Document and communicate study results, technical findings, and recommendations to global cross-functional teams, including U.S.-based stakeholders.

What you'll need:

  • B.Sc. or M.Sc. in Biomedical Engineering or any other relevant field.
  • 2-3 years of professional experience in the medical industry
  • Strong problem-solving, organizational, analytical, and critical thinking skills.
  • Ability to independently plan and execute work with a high level of ownership and accountability
  • Excellent organizational skills and the ability to manage multiple priorities in a dynamic, hands-on R&D environment.
  • Strong written and verbal communication skills in English.
  • Experience with data analysis tools (e.g., MATLAB, Python, Minitab, or similar).
  • Programming experience is an advantage.
  • Fluent in English, both written and spoken.
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