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Mechanical Design Engineer

Job in Palo Alto, Santa Clara County, California, 94306, USA
Listing for: Sira Consulting, an Inc 5000 company
Full Time position
Listed on 2026-10-18
Job specializations:
  • Engineering
    Manufacturing Engineer, Mechanical Engineer, Product Engineer, Quality Engineering
  • Manufacturing / Production
    Manufacturing Engineer, Product Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 120000 - 170000 USD Yearly USD 120000.00 170000.00 YEAR
Job Description & How to Apply Below
  • Design mechanical components, assemblies, and systems for medical devices from concept to production using Creo & Solid Works.
  • Hands-on experience in PDM / PLM (SAP-ECTR) for managing lifecycle of the components, managing ECO / ECR (SAP).
  • Build and test prototypes to validate design performance against specifications and ensure safety and reliability.
  • Select appropriate materials by considering factors critical in the medical industry, such as biocompatibility, sterilization compatibility, and cost-effectiveness.
  • (DFM/DFA):
    Designs are optimized to ensure they can be efficiently produced and assembled, considering manufacturing processes.
  • Using advanced CAD software such as Creo or Solid Works, create detailed 2D drawings of components and assemblies.
  • Apply Geometric Dimensioning and Tolerancing (GD&T) to communicate design tolerances and specifications precisely for accurate manufacturing.
  • Generate and maintain the BOM, which is a comprehensive list of all raw materials, components, and assemblies needed to manufacture the final product.
  • Organize and maintain a comprehensive Design History File (DHF), which documents the entire design process, including inputs, outputs, verification, and validation records.
  • Revising and updating technical drawings and documentation as needed and for managing the engineering change order (ECO) process.
  • Ensuring all design and documentation adheres to strict medical device regulations from bodies like the FDA and standards like ISO 13485.
  • Work with a range of professionals, including quality assurance, regulatory affairs, manufacturing and sourcing, to bring a product from concept to launch.
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