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Design Engineer

2 - 7 years

2 - 3 Lacs

Posted:3 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

We are seeking a Design Engineer with a Mechanical Engineering background to work on product
design and development. The ideal candidate should have expertise in SolidWorks and experience in designing components for the medical device, biotech, or life sciences industry.

Designation:

Design Engineer

Department:

Product Design & Development

Experience:

Minimum 2 years in design engineering

Industry/Background:

Mechanical / Medical Device / Pharma / Lifesciences Industry

Software Expertise:

SolidWorks (mandatory), AutoCAD (preferred)

Qualification:

B.E / B.Tech Mechanical Engineering or related field

Employment Status:

Permanent

Workplace Type:

On-site

Minimum Requirements:

  • Minimum 2 years of experience in product design and development.
  • Strong proficiency in SolidWorks for 3D modeling, drafting, and assembly design.
  • Experience in designing plastic and metal components, sheet metal, and machined parts.
  • Knowledge of GD&T, tolerance analysis, and material selection.
  • Understanding of manufacturing processes, prototyping, and DFM/DFA principles.
  • Ability to read and interpret engineering drawings.
  • Exposure to ISO 13485 and medical device design standards is a plus.
  • Strong problem-solving and analytical skills.
  • Good communication and teamwork skills.

Roles and Responsibilities:

  • Design and develop medical devices and accessories as per industry standards.
  • Create and modify 3D models, technical drawings, and assemblies using SolidWorks.
  • Conduct DFM (Design for Manufacturing) and DFA (Design for Assembly) analysis.
  • Work closely with R&D, production, and quality teams to ensure product feasibility.
  • Prepare technical documentation, BOMs, and design reports.
  • Collaborate with vendors and suppliers for prototyping and manufacturing feasibility.
  • Support testing, validation, and regulatory documentation for product approvals.
  • Ensure compliance with ISO 13485 and regulatory standards for medical devices.

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