Design Engineer

What You Will Do

Product Support & Sustaining Engineering – Provide engineering support for existing medical devices (Hip & Knee portfolio), ensuring reliability, quality, and compliance with regulatory standards.

Design & Process Improvements – Identify and implement design and process changes to improve product performance, manufacturability, and cost-effectiveness.

Root Cause Analysis & Troubleshooting – Investigate product issues, perform root cause analysis, and develop corrective and preventive actions.

Regulatory Compliance & Documentation – Ensure all design changes comply with global regulatory requirements (FDA, ISO, MDR, etc.) and update design history files (DHF).

Testing & Verification – Conduct testing, data analysis, and validation of product changes in collaboration with quality and regulatory teams.

Cross-functional Collaboration – Work with manufacturing, quality, supply chain, and R&D teams to ensure seamless implementation of product changes.

Supplier & Component Management – Evaluate and qualify alternative components or suppliers to support product continuity and cost reduction.

Risk Management – Assess potential risks associated with design changes and implement necessary mitigations.

Change Control & Project Execution – Drive Engineering Change Orders (ECOs), work within PLM systems, and ensure timely execution of sustaining projects.

What You Need:

Must Have qualifications:

Strong problem-solving skills 

2-4.5 years of solid understanding of Design fundamentals.Good understanding of Drawing drafting

Hands-on experience in 3D modeling softwares (Solidworks, Creo, NX etc.)

Product development process GDT Team player, Solid communicator 

Good to have:

Statistics, Hands-on exposure to V&V activities , FEA