Highlights

These activities may include the following: developing product specifications, performing robust design evaluation, creating risk analyses, meeting goals for design reviews, and setting & executing design verification and validation strategies. The Senior R&D Engineer is responsible for the design and development of new and improved products and procedures that address vascular diseases and conditions using minimally invasive techniques.

Numbers & Facts

LocationMenlo Park, CA

Description

SUMMARY

The Senior R&D Engineer is responsible for the design and development of new and improved products and procedures that address vascular diseases and conditions using minimally invasive techniques.


PRINCIPAL DUTIES AND RESPONSIBILITIES

  • Design, prototype and develop novel design solutions for catheter-based products to improve performance and ease of use in clinical procedures.
  • Work as part of a cross-functional team to develop and evaluate product designs through verification and validation testing
  • Prepare technical documentation, including manufacturing instructions, test methods, protocols, and reports to support design control activities and regulatory submissions
  • Provide periodic updates regarding project status
  • Contribute to the company's intellectual property via invention disclosures, brainstorming sessions, and prototypes to demonstrate reduction to practice
  • Interact with physicians regarding product development, testing, and product demonstrations
  • Train other team members on product assembly; troubleshoot assembly process issues
  • Maintain Design Control activities for new product development from initial concept through commercialization. These activities may include the following: developing product specifications, performing robust design evaluation, creating risk analyses, meeting goals for design reviews, and setting & executing design verification and validation strategies.
  • Work collaboratively with other company functions as needed, including R&D, Marketing, Operations, Quality, Clinical and Regulatory to ensure project success.
  • Support the development and upkeep of the Company's Quality System in conjunction with the Company's Quality Department.


EXPERIENCE REQUIREMENTS

  • At least 5 years' experience leading development of disposable medical device products.
  • Experience with design and process development of medical device catheters.
  • Experience with FDA and ISO standards for medical device design controls and manufacturing


EDUCATION REQUIREMENTS

BS Engineering (Mechanical or Biomedical)


OTHER QUALIFICATIONS

  • Working knowledge of common catheter materials and construction methods.
  • Successful track record of developing medical disposable products from conceptualization through product launch
  • Self-motivated with ability to work independently and with minimal supervision

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