Staff R&D Project Engineer - JJMT Electrophysiology at Johnson Johnson
Irvine, CA 92618, USA -
Full Time


Start Date

Immediate

Expiry Date

15 Oct, 25

Salary

0.0

Posted On

16 Jul, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Chemistry, Solidworks, Consideration, Precious Metals, Veterans, Design, Biology, Nitinol, Manufacturing Techniques, Color, Cardiac Electrophysiology, Disabilities, Support Center, Physics, Polymers, Biomedical Engineering

Industry

Electrical/Electronic Manufacturing

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at https://www.jnj.com

JOB DESCRIPTION:

Johnson & Johnson MedTech, Electrophysiology, is recruiting an Staff R&D Project Engineer located in Irvine, California. This role is on-site with flexibility for a hybrid schedule.
Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through 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 humanity. Learn more at https://www.jnj.com/.
Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.
Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
The Staff R&D Project Engineer provides engineering and design services to Advanced R&D. The Senior Research & Development project Engineer will be supporting project teams in the development of electrophysiology catheters and systems at JJMT - Electrophysiology. Project support is across all stages of product development process includes overall design, requirement development, design for manufacturing, test method development, and product verification and validation testing.

QUALIFICATIONS:

Required:

  • A minimum of a BS in physics, chemistry, biology, mechanical, electrical, biomedical engineering, or related field
  • A minimum of 4+ years of engineering work experience, with 3+ years of experience in the medical device industry
  • Ability to travel up to 10%, domestic and international

Preferred:

  • Knowledge of geometric dimensioning and tolerancing (GD&T)
  • Strong knowledge of CAD software including SolidWorks
  • Able to interpret 2D engineering drawing
  • Previous experience in cardiac electrophysiology
  • Previous experience working with physicians
  • 2+ years of R&D experience
  • Understanding of quality standards pertaining to medical device
  • Experience with statistical analysis and design of experiments (DOE)
  • Knowledge of engineering materials such as nitinol, precious metals, and/or polymers and manufacturing techniques related to the materials
  • A minimum of 1 year of experience working in a pre-clinical or clinical environment

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.

Responsibilities
  • Supports engineering by researching, designing, developing, and testing according to established policies, procedures, government and compliance regulations, and customer requirements.
  • Develop customer requirements and product specifications with validated test methods
  • Builds prototypes and works with the lab to develop test fixtures
  • Performs failure analysis, verification testing and generation of test reports for modules or subsystems.
  • Support quality improvement initiatives such as process and product characterizations that lead to continuous / cost improvements.
  • Interact with vendors and work with component quality team toward full qualification of components.
  • Expected to assist in the writing of reports, work instructions, test methods and procedures
  • Optimizes processes for initial and long-term scaling of new designs and processes for the designs
  • Works directly with other engineers and skilled technicians to build and optimize designs
  • Tests design prototypes and modifies design based upon test results
  • Participates in in vitro and in vivo device testing
  • Documents design and performs testing for V&V activities
  • Leads the transfer of designs from concept to pilot to full production
  • Works with cross-functional team including, quality, medical affairs, regulatory, manufacturing, … teams toward completion of all project deliverables
  • Responsible for communicating business related issues or opportunities to next management
  • Responsible for ensuring personal and Company compliance with all Federal, State, local and
  • Company regulations, policies, and procedures
  • Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable
  • Performs other duties assigned as needed
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