Work Flexibility: Hybrid
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 draftingHands-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 , FEATravel Percentage: None