Senior Engineer I, Research and Development - FEA
About this role
Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $101,300.00 - $101,300.00 SalaryJob Title: Senior Engineer, Research and Development - FEA
Senior Engineer I, Research and Development - FEA
Senior Engineer II, Research and Development - FEA
Senior Engineer III, Research and Development - FEA
Role Level: Individual Contributor
Supervisor/Manager Title: Director, Research and Development, Valves
Job Location & Environment: Irvine, CA – Corporate Office Environment, R&D Lab
Job Description Summary: Responsible for supporting the development of subsystems and components for transcatheter heart valve and delivery system using Finite Element Analysis (FEA) and test method development.
Job Responsibilities
Develop and validate test methods for components (nitinol, viscoelastic material like porcine pericardium etc.) or subsystems for transcatheter heart valves and delivery systems in accordance with quality system requirements.
Develop and validate FEA models for components (nitinol, viscoelastic material like porcine pericardium etc.) or subsystems for transcatheter heart valves and delivery systems in accordance with quality system requirements.
Design and document components and subsystems.
Procure components.
Develop assembly procedures.
Conduct engineering analysis and feasibility testing of components of subsystems to ensure proper fit and function.
Partner with Quality to conduct risk analysis and develop and execute design verification activities.
Partner with Manufacturing to develop manufacturing procedures and processes and transfer the product to external manufacturing houses.
QualificationsRequired Education and Experience
A Bachelor of Science degree in Mechanical or Biomedical Engineering (or equivalent engineering degree) is required.
Minimum of 5+ years’ experience in R&D or product development of medical devices, pharmaceutical or life sciences product technology. Level I, II, III DOE.
Minimum of 3 years of experience in FEA is required.
Minimum of 3 years of experience with Abaqus and/or equivalent software is required.
Knowledge of the product development process and applicable Quality System requirements in the medical device industry is required.
Skills and Abilities Required for This Job
Must be able to work effectively and collaborate within cross-functional teams.
Must be able to effectively articulate (verbally and in writing) results and conclusions to technical and non-technical personnel.
Must have strong documentation skills.
Must take initiative and be able to conduct hands-on work.
Must be able to handle multiple tasks with high attention to detail.
Physical Requirements
Ability to sit or stand for extended periods while working at a computer or in meetings.
Ability to work in a laboratory and/or manufacturing environment, including wearing appropriate PPE.
Ability to move between office, lab, and manufacturing floor environments as needed.
Company at a glance
JenaValve is a medical device company developing the first transcatheter heart valve technology that is uniquely designed for the minimally invasive treatment of aortic regurgitation (AR).
The JenaValve Trilogy Heart Valve System is the first and only device currently approved in the EU for the treatment of severe, symptomatic aortic regurgitation in patients that are deemed high-risk for surgical aortic valve replacement. The Trilogy System is also CE-Mark approved for treatment of severe, symptomatic aortic stenosis.
In the US, JenaValve has completed enrollment of the ALIGN-AR IDE Clinical Trial which will support a future PMA submission. If approved, the Trilogy System would become the first and only TAVR system in the US indicated for the treatment of symptomatic, severe AR.
JenaValve is headquartered in Irvine, California with offices in Leeds, U.K. and Munich, Germany.
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