Engineer II, R&D

Edwards Lifesciences is seeking a highly skilled engineer to join our Implant R&D team playing a key role in advancing THV Commercial Portfolio Excellence (CPEx) initiatives, supporting activities ranging from feasibility assessments and design verification (DV) testing to indication expansions and Global Supply Chain (GSC) scalability efforts. By partnering closely with cross-functional teams, you will generate critical data and insights that drive technical decisions, shape device performance, and ultimately improve patient outcomes. This position offers a unique blend of hands-on valve testing, product development, and innovation-focused engineering activities within a highly collaborative R&D organization.

• Own test plans for evaluating the performance of transcatheter heart valve designs. Deliver credible evidence enabling assessment of hemodynamic performance, durability, resistance to embolization, and interactions with delivery catheter system and patient anatomy under clinically relevant use conditions.
• Apply knowledge of transcatheter valve replacement techniques to interrogate intraprocedural valve performance and predict valve performance throughout the intended lifecycle of the device.
• Author documentation to support product development and product change assessment submissions within Edwards’ design control framework. You will write and release design verification plans, protocols, execute tests, direct the activities of technicians, analyze data, and author reports.
• Generate work instructions, test methods, engineering drawings/prototypes, etc. to establish/characterize product and/or process specifications.
• Collaborate with experts to develop an understanding of anatomy-device and device-device interactions. Use this data to develop test fixtures and methods to challenge valve performance under complex and novel use conditions to support indication expansion projects. Experience with CAD design and drawings as well as manufacturing techniques (molding, machining, 3D printing) is preferred.
• Experience with traditional engineering materials (plastics, metals, etc.) as well as biomaterials (pericardial tissue) is preferred.
• Collaborate effectively with cross-functional partners including Delivery System R&D, Manufacturing, Quality Engineering, Regulatory Affairs, and Clinical Development to ensure alignment on performance assessment strategies, results, and interpretation.
• Employ statistical techniques to design test strategies to with the appropriate level of confidence based on an assessment of risk. Use statistical tools such as ANOVA, multivariate regression, and measurement system analysis (MSA) to interpret empirical results with an understanding of the associated uncertainty and implications for hypothesis testing.
• Communicate your ideas and findings effectively including authoring reports and technical summaries for regulatory submissions, preparing and delivering presentations to cross-functional stakeholders, and collaborating and coordinating with colleagues at all levels including other engineers, technicians, and leadership.
• Document methodologies and findings in compliance with internal standards and regulatory requirements.

• Bachelor's Degree in Engineering or Scientific field, 2 years experience Required

OR

• Master's Degree or equivalent in Engineering or Scientific field with internship, senior projects, or thesis in Engineering or Scientific field

• Hands-on experience with test method development, fixture design, in-lab test execution, and data analysis.
• Strong problem-solving and critical thinking skills.
• Excellent verbal communication and collaboration skills in a cross-functional environment, including proficiency with MS PowerPoint.
• Strong documentation and technical writing skills including proficiency with Microsoft Word.
• Familiarity with regulatory standards (ISO, FDA) and design control processes.
• Ability to work well independently and as a team member & build productive internal/external working relationships.
• Ability to manage competing priorities in a fast paced environment.
• Strong understanding of statistical techniques and engineering tools such as MS Excel, Minitab, and SolidWorks.
• Engineering experience in a regulated industry, preferably in cardiovascular implantable devices. Experience with testing heart valves in compliance with the ISO 5840 standard is preferred.
• Familiarity with product lifecycle management (PLM), document control, and Windchill.
• Experience with authoring deliverables require for regulatory submissions to regulatory authorities including the FDA.

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 (CA), the base pay range for this position is $87,000 to $123,000(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.