R&D Engineer

Zeus

San Jose, CAOn-siteFull time
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Location
San Jose, CA
Work style
On-site
Job type
Full time
Posted
Nov 3
1 day ago
Career path

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About the company

Zeus

Plastics · 1,001 to 5,000 employees

Zeus on LinkedIn

What you'll do

  • Perform aspects of product design and development
  • Address customer needs for a complete procedural solution
  • Plan, organize and direct engineering staff
  • Meet objectives for design, new product development and improvement of existing product lines

What you need

  • Bachelor’s Degree in Mechanical or Biomedical Engineering is required.
  • Master's Degree in Mechanical or Biomedical Engineering is preferred.
  • Must have three (3) plus years’ relevant Engineering experience
  • Knowledge and experience in catheter design is required.
  • Experience with CAD software such as AutoCad or Solidworks is required.
  • Knowledge and experience in development processes and in documentation writing is required.
  • Experience with statistical analysis and design of experiments (DOE) preferred.
  • Ability to use PC and associated software is required.
  • In-depth knowledge of material and metals is preferred.
  • Knowledge of Good Manufacturing Process and Good Documentation Practice.
  • Values: Integrity, Accountability, Teamwork, Innovation
  • Excellent verbal and written communication skills
  • Ability to work independently
  • Ability to manage tight timelines and changing priorities
  • Excellent problem -solving techniques
  • Proficient with Microsoft office applications
  • Skilled at providing technical leadership on cross-functional teams

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See full description on company page, apply now

Read the full posting here
JOB OVERVIEW This position is responsible for aspects of the product design and development of a project with a focus on innovative medical devices that address the customer needs for a complete procedural solution. The engineering manager plans, organizes and directs engineering staff to meet company objectives for design, new product development and improvement of existing product lines by performing the following duties personally or through subordinates. This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS).

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