Key Responsibilities :
1. Design & Product Development
- . Lead the design and development of new products and improvements to existing devices
using SolidWorks and AutoCAD.
. Translate clinical and market requirements into functional designs while ensuringmanufacturability and cost-effectiveness.
. Validate engineering calculations, tolerance stack-ups, and material selection forimplantable devices and surgical instruments.
2. Project Leadership
. Plan and execute design activities in alignment with project timelines.. Coordinate design reviews, risk analysis, and design verification / validation.. Collaborate with the D&D Head to define design strategy and resource allocation.3. Mentorship & Team Development
. Guide and mentor Junior Design Engineers in modeling, drafting, design analysis, anddocumentation.
. Review work submitted by junior staff and provide constructive feedback.4. Manufacturing Integration
. Ensure designs are optimized for manufacturing processes such as CNC machining, lasermarking, anodizing, and PEEK / titanium-specific considerations.
. Work closely with production, quality, and supply chain teams to ensure smooth handoverfrom design to production.
5. Regulatory & Documentation
. Prepare and review Design History Files (DHF), Technical Files, Risk Management Reports,and Engineering Change Requests (ECRs).
. Ensure all designs and documentation meet CE MDR, US FDA, and CDSCO regulatoryrequirements.
. Support audits and regulatory submissions with accurate and complete documentation.6. Design Evaluation & Predicate Comparison
. Conduct design benchmarking and engineering justification reports.. Compare new designs against predicate or competitive devices for clinical and functionalperformance.
7. Innovation & Continuous Improvement
. Research new design trends, technologies, and surgical techniques in arthroscopy andorthopedics.
. Contribute to IP development, design patents, and publications where applicable.Skills Required
Solidworks, Titanium, Cnc Machining, Anodizing, Autocad