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Staff Engineer , THV Research and Development-THV

Job in Irvine, Orange County, California, 92713, USA
Listing for: Jenavalve Technology
Full Time position
Listed on 2026-07-07
Job specializations:
  • Engineering
    Product Engineer, Quality Engineering, Research Scientist
Salary/Wage Range or Industry Benchmark: 134100 USD Yearly USD 134100.00 YEAR
Job Description & How to Apply Below
Position: Staff Engineer I, THV Research and Development-THV

Job Details

Job Title:

Staff Engineer, THV Research and Development

Job Location:

Irvine, CA 92618

Position Type:
Full Time

Education Level: 4 Year Degree

Salary Range: $ - $

Supervisor/Manager

Title:

Director, Research and Development

Job Description Summary

Responsible for the development of novel subsystems and components for transcatheter heart valves and/or delivery systems.

Job Responsibilities
  • Conceive, design, and develop components and subsystems of moderate/high complexity for transcatheter heart valves and/or delivery systems in accordance with quality system requirements and with minimal supervision.
  • Create, review and/or approve component and subsystem drawings/specifications and documentation.
  • Identify/evaluate vendors, procure components and develop component specifications.
  • Develop test methods, conduct testing, and interpret data.
  • Conduct engineering analyses and feasibility testing of components and subsystems to ensure proper fit and function.
  • Conduct competitive product evaluation and product failure analyses.
  • Partner with Quality to conduct risk analyses and develop/execute design verification activities.
  • Partner with Manufacturing to develop manufacturing processes, tooling/fixtures, and transfer product/processes to manufacturing.
  • Supervise R&D Technicians.
Qualifications
  • A Bachelor of Science degree in Engineering or Technical discipline with related work experience.
  • Minimum of 6+ years’ experience in R&D or product development of medical devices, pharmaceutical or life science product technology. Level I, II, III DOE.
  • Familiarity with 21

    CFR
    820 and ISO 13485 requirements.
  • Knowledge of the product development process and applicable Quality System requirements in the medical device industry.
  • Demonstration of ability to work effectively and collaborate within cross-functional teams.
  • Demonstration of ability to effectively communicate (in oral presentation and written documentation) test protocols, reports, and technical summaries to technical and non-technical personnel.
  • Hands-on experience in product development within an R&D lab environment.
Skills and Abilities
  • Ability to work independently and in collaboration within cross-functional teams.
  • Ability to manage multiple tasks in a timely manner with high attention to detail.
  • Ability to build strong relationships at all levels of the organization, cross-functionally and with key external personnel.
  • Demonstrated strength in problem analysis, judgment, decision making and critical thinking.
  • Strong written and verbal communication.
  • Experience in developing product specifications based on user needs and writing design verification and validation protocols.
  • Strong Solidworks/CAD skills.
  • Project management skills.
  • Knowledge of statistical analysis and applications.
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