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Sr R&D Engineer

Zeus Industrial Products, Inc.
San Jose, USA
Full-time
Senior
Onsite
Discovered 5 days ago
autocadsolidworks

Full Job Posting

QUALIFICATIONS:

  • Bachelor’s Degree in Mechanical Engineering is required.
  • Master's Degree in Mechanical or Biomedical Engineering is preferred.
  • Must have five (5) 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 required.
  • Knowledge of Good Manufacturing Process and Good Documentation Practice.
  • COMPENTENCIES: To perform the job successfully, an individual should demonstrate the following competencies:
  • 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
  • Pay range is $151,000-$189,000

Responsibilities

  • ESSENTIAL FUNCTIONS:
  • Support R&D team to design and test catheters and delivery systems
  • Develop concepts, designs and details for machines, tools and fixtures.
  • Support includes overall design, design for manufacturing, test method development, and product verification and validation testing
  • Lead technical discussion and decision making with cross functional team.
  • Interface between external vendors and core team.
  • Develop specifications, engineering blueprints and detail drawings.
  • Resolve design problems related to material characteristics, dimensional tolerances, service requirements, manufacturing procedures, and cost.
  • Provide design changes for existing products. Ensures proper documentation of changes.
  • Create engineering designs, develop plans and keep laboratory notebooks on all work.
  • Conduct testing (Bench, V&V, in vivo); develop and utilize test protocols; generate written reports.
  • Travel to customer sites, domestic and international, to gather VOC, perform testing and/or perform troubleshooting activities.
  • Responsible for performing design reviews and pre-validation assessments to ensure the safe and environmentally sound processes and designs.
  • Responsible for the purchase or design of equipment that meets health, safety and environmental standards set by the company.
  • Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures.
  • Responsible for communicating business related issues or opportunities to next management level.
  • Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition.
  • Performs other duties assigned as needed.
  • SUPERVISOR RESPONSIBILITIES:
  • The position does have supervisor responsibilities, is responsible for performance management and the hiring of the employees that are designated under their supervision.

Preferred Qualifications

  • Master's Degree in Mechanical or Biomedical Engineering is preferred.
  • Experience with statistical analysis and design of experiments (DOE) preferred.

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