CAD Engineer (Medical Devices)

Infosys; Maharashtra; On-site; INR 600,000 - 900,000; Full time

Job summary

Infosys in India is seeking a Mechanical Design Engineer to develop 3D models and detailed manufacturing drawings using SolidWorks. You will apply DFM and DFA principles to optimize designs for manufacturing and assembly, perform tolerance analyses, and create engineering documentation including BOMs.

You will collaborate with Manufacturing, Quality, R&D and Suppliers, support prototyping and testing, manage design data in PLM/PDM systems, ensure compliance with medical device standards, and

Qualifications

• Proficient in SolidWorks CAD design and drafting.
• Experience with GD&T and tolerance stack-up analysis.
• Knowledge of DFM/DFA for medical device manufacturing.

Responsibilities

• Develop 3D models, assemblies, and detailed drawings using SolidWorks.
• Apply DFM/DFA principles to optimize designs for manufacturing and assembly.
• Perform engineering calculations, tolerance analysis, and design validations.

Skills

SolidWorks CAD

GD&T

Tolerance analysis

DFM

DFA

Problem solving

Analytical skills

Cross-functional collaboration

Manufacturing processes knowledge

Tools

PLM/PDM software

Job description

Strong experience in Mechanical Design Engineering. Hands-on expertise in SolidWorks CAD Design. Knowledge of DFM (Design for Manufacturability) and DFA (Design for Assembly). Experience in GD&T and tolerance stack-up analysis. Knowledge of engineering calculations and mechanical design principles. Understanding of manufacturing processes such as machining, injection molding, sheet metal, and assembly. Experience with PLM/PDM software. Strong problem-solving and analytical skills.

Develop 3D models, assemblies, and detailed manufacturing drawings using SolidWorks. Apply DFM & DFA principles to optimize product designs for manufacturing and assembly. Perform engineering design calculations, tolerance analysis, and design validations. Create and maintain engineering documentation, BOMs, and design records. Conduct GD&T (Geometric Dimensioning & Tolerancing) and tolerance stack-up analysis. Collaborate with cross-functional teams including Manufacturing, Quality, R&D, and Supplier teams. Support prototype development, testing, and product improvements. Work with PLM/PDM systems for design data management and revision control. Ensure compliance with Medical Device industry standards and design regulations. Assist in product lifecycle activities from concept to production release.

Experience in the Medical Devices industry. Familiarity with product development processes and regulatory requirements. Knowledge of risk management and quality standards within medical device manufacturing. Experience working with multidisciplinary product development teams.