System Engineer

TechDigital Group

Palo Alto (CA)

On-site

USD 60,000 - 100,000

Full time

14 days+

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Job summary

An established industry player is seeking a talented Mechanical Engineer to join their innovative team in Palo Alto. This role involves designing and drafting sheet metal components using advanced CAD tools such as SOLIDWORKS and Creo. You'll be responsible for developing prototypes, conducting performance testing, and ensuring compliance with medical device standards. If you have a passion for mechanical design and a commitment to quality, this opportunity offers a chance to contribute to exciting projects in a collaborative environment. Join a forward-thinking company dedicated to continuous improvement and excellence in engineering.

Qualifications

  • Proficient in CAD tools for designing sheet metal components.
  • Strong understanding of GD&T and tolerance analysis.

Responsibilities

  • Design and prototype mechanical components based on specifications.
  • Conduct testing of prototypes and document results.

Skills

CAD Design
Geometric Dimension & Tolerancing (GD&T)
Tolerance Stack Up Analysis
Functional Testing
BOM Management
Technical Documentation

Education

Bachelor's Degree in Mechanical Engineering

Tools

SOLIDWORKS
Creo
SAP

Job description

  • Design and drafting of sheet metal components using CAD tools like SOLIDWORKS and Creo.
  • Development and prototyping of mechanical components based on design specifications.
  • Experience / good understanding of Geometric Dimension & Tolerancing (GD&T).
  • Experience in Tolerance stack up analysis.
  • Conduct functional and performance testing of prototypes and document results.
  • Create and manage BOMs (Bill of Materials) and engineering change requests in SAP.
  • Ensure compliance with design standards, safety regulations, and quality requirements.
  • Support continuous improvement initiatives related to product design and manufacturing processes.
  • Ensure compliance with medical device standards and regulations (e.g., ISO 13485, FDA).
  • Prepare and maintain technical documentation for design history files (DHF).
  • Collaborate with multi cross-functional teams for design reviews and manufacturing feasibility.
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