drjobs Principal R&D Engineer (Sustaining) - Shockwave

Principal R&D Engineer (Sustaining) - Shockwave

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1 Vacancy
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Job Location drjobs

Santa Clara - USA

Monthly Salary drjobs

$ 141000 - 227000

Vacancy

1 Vacancy

Job Description

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for more at

Job Function:

R&D Product Development

Job Sub Function:

R&D Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Santa Clara California United States of America

Job Description:

Johnson & Johnson is hiring for aPrincipal R&D Engineer (Sustaining) Shockwave to join our team located in Santa Clara CA.

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments. Ready to join a team thats pioneering the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. Our Shockwave Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the treatment of calcified plaque.

Position Overview

The Principal R&D Engineer will use technical and leadership skills in the development and sustaining of innovative products to treat arterial disease. The Principal R&D Engineer will participate on multiple cross-functional teams that manage projects in support of base business and development.

Essential Job Functions

  • Provide technical leadership for projects in coronary and peripheral artery space.
  • Provide mentorship to other engineers and assignments to technicians as required.
  • Develop and maintain technical documentation such as drawings for equipment fixtures components and assemblies for manufacturing processes.
  • Supports pilot manufacturing as well as commercial production
  • Support commercial products as subject matter expert on product design including design changes and regulatory inquiries.
  • Prototype and develop proof of concept designs and test methods based on the defined user needs and requirements.
  • Represent R&D in cross-functional teams that drive geographical expansion of products.
  • Solve challenging and complex technical problems during the new product development process and in support of commercial products.
  • Analyze evaluate source and coordinate the procurement of new materials to support prototyping and pilot operation.
  • Develop protocols/reports and perform product assessment as well as verification and validation testing.
  • Perform process-related design tasks to support pilot manufacturing utilizing Design for Manufacturing principles and working with assemblers to ensure robust processes.
  • Identify suppliers and maintain relationships to ensure the delivery of superior components and services.
  • Enhance the intellectual property position of the company via invention disclosures and patent applications.
  • Participate as SME or core team member on product development team(s) that manage projects from concept through commercialization.
  • Design and develop product(s) in compliance with the companys Design Control requirements and consistent with applicable regulatory requirements.
  • Ensure proper documentation consistent with companys quality system.
  • Responsible for knowing and planning activities consistent with the companys quality policy and quality objectives.
  • Maintain current knowledge of competitive technologies in addition to medical technical and biomedical developments related to companys products.
  • Support company goals and objectives policies and procedures Quality Systems and FDA regulations.
  • Other duties as assigned.

Requirements

  • Bachelors Degree in Mechanical or Biomedical Engineering and 10 years experience in engineering OR a Masters Degree and 8 years experience in engineering.
  • Experience in early-stage catheter and/or lead based cardiovascular device development.
  • Knowledge of disposable structural heart device design material selection and testing is a strong plus.
  • Strong understanding of engineering materials component selection and design for reliability and manufacturability.
  • Strong understanding of statistics including design of experiments Gage R&R capability etc. is a strong plus.
  • Strong teamwork skills and demonstrated ability to work closely with cross functional partners.
  • Effective communication skills with all levels of management and organizations.
  • Operate independently and adaptability to changing requirements.
  • Ability to work in a fast-paced environment managing multiple priorities.
  • Employee may be required to lift objects up to 25 lbs.

Additional Information:

The anticipated salary range for this position is $141000-$227000

The Company maintains highly competitive performance-based compensation programs. Under current guidelines this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporations performance over a calendar/performance year. Bonuses are awarded at the Companys discretion on an individual basis.


Required Experience:

Staff IC

Employment Type

Full-Time

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