Johnson & Johnson - Irvine, CA

posted about 2 months ago

Full-time - Mid Level
Irvine, CA
Chemical Manufacturing

About the position

The Senior Engineer, R&D position at J&J MedTech in Irvine, CA, focuses on supporting catheter and sheath engineering projects for the development of a new left atrial appendage (LAA) closure system. The role involves working within a dynamic team to design, document, and prototype new products, ensuring compliance with health and safety regulations while fostering innovation in medical device technology.

Responsibilities

  • Support the design of new/existing components while ensuring all design requirements are met.
  • Develop and execute test methods, procedures, work instructions, and reports with little supervision.
  • Implement complex design concepts and ideas into working drawings, solid models, and prototypes.
  • Study specifications, engineering blueprints, tool orders, and shop data to resolve design problems.
  • Develop concepts, designs, and details for machines, tools, and fixtures.
  • Assist with the inspection of components and fixtures after fabrication to ensure they meet specifications.
  • Interface between external vendors and internal core team members.
  • Prototype design and perform feasibility assessments at a rapid pace.
  • Conduct complex or novel assignments requiring the development of new or improved techniques or procedures.
  • Work hands-on to manufacture and evaluate the feasibility of prototypes.
  • Ensure compliance with all Federal, State, local and company regulations, policies, and procedures for Health, Safety, and Environmental compliance.

Requirements

  • A minimum B.S. in Mechanical or Biomedical Engineering or equivalent with industry experience.
  • Experience with CAD software (Solidworks, Creo or similar) is required.
  • Collaborative teammate with strong communication skills, both written and verbal.
  • Ability to come up with creative solutions to solve technical issues.
  • General understanding of concept development, 3D modeling, creating 2D drawings, GD&T, and manufacturing methods.
  • Ability to work with outside vendors for procuring parts.

Nice-to-haves

  • M.S. in Mechanical or Biomedical Engineering or higher education.
  • Ability to write and communicate clearly, including generating and presenting well-written reports.
  • General understanding of test method development, setup, and execution along with equipment setup and validation.
  • Prior experience with inspection of components.
  • Medical Device experience with 4+ years of experience.
  • Structural heart experience highly preferred.
  • Experience with nitinol related devices.
  • Knowledge and experience in product development processes.
  • Experience with statistical analysis.

Benefits

  • Health insurance coverage
  • Dental insurance coverage
  • Vision insurance coverage
  • 401k retirement savings plan
  • Paid holidays
  • Paid time off (PTO)
  • Employee discounts
  • Professional development opportunities
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