Medical Devices Design Engineer

Role overview

Medical Devices Design Engineer at Cyient

Collaborate with Quality, Regulatory, Systems Engineering, Manufacturing, Supplier Quality, Clinical, Human Factors, Sourcing, and Project Management teams.

Responsibilities

• 1.
• Design and develop electromechanical medical devices, including mechanical subsystems, precision components, assemblies, and associated accessories from concept through production. 2.
• Develop innovative product concepts, detailed 3D CAD models, assemblies, engineering drawings, tolerance analyses, bills of materials, material specifications, and technical documentation. 3.
• Build, source, and evaluate prototypes through rapid prototyping, prototype tooling, and representative manufacturing processes; analyse prototype performance and use results to improve product design, reliability, usability, and manufacturability. 4.
• Apply Design for Manufacturability (DFM) and Design for Assembly (DFA) principles to optimize component design, assembly processes, product quality, reliability, and cost. 5.
• Perform engineering analyses, including design calculations, tolerance stack-up analysis, FEA and CFD, where applicable, to evaluate strength, fatigue, thermal performance, fluid flow, and durability. 6.
• Lead design reviews, DFMEA, risk assessments, root-cause analysis, failure analysis, and corrective actions to identify and mitigate product, subsystem, component, interface, and manufacturing risks. 7.
• Develop engineering test strategies, test fixtures, and reports to support prototype evaluation, design verification, reliability testing, usability activities, and product validation. 8.
• Maintain design-control and product-lifecycle documentation, including requirements, design inputs and outputs, change-control records, Engineering Change Orders, and technical reports. 9.

Required qualifications

• Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, or a related engineering discipline with 8+ years of experience in medical product design and development. 2.
• Strong proficiency in parametric 3D CAD software, preferably Creo & SolidWorks with experience creating 3D models, detailed engineering drawings, assembly definitions, bills of materials, and production-ready design documentation. 3.
• Practical experience applying DFM and DFA principles to precision machining, injection moulding, sheet metal, casting, forging, surface finishing, coatings, and joining methods. 4.
• Knowledge of FDA requirements, European MDR expectations, ISO 13485, ISO 14971, and other applicable medical-device quality and regulatory practices. 5.
• Strong communication, technical documentation, innovation, stakeholder-management, and cross-functional collaboration skills, with experience supporting NPI, manufacturing transfer, product design support, and the complete product lifecycle; 6.
• Orthopaedic or dental product-development experience is an added advantage.

Employment details

• Location: Hyderabad

Additional role details

• Role and