8+ years of mechanical design and development experience in medical device NPD.
Experience leading mechanical development of electromechanical products through the full product lifecycle in regulated environments.
Bachelor's or Master's degree in Mechanical Engineering.
Strong proficiency in CAD tools like SolidWorks or Creo.
In-depth understanding of materials, manufacturing processes, and electromechanical integration.
Responsibilities
Act as technical lead for mechanical design in medical device programs.
Own and oversee mechanical architecture and interfaces for electromechanical subsystems.
Lead mechanical design from concept through production release.
Translate user needs and system requirements into mechanical designs.
Develop and review 3D CAD models, detailed drawings, and BOMs.
Integrate components such as motors and sensors within mechanical assemblies.
Lead risk management activities and ensure compliance with standards.
Benefits
Mentorship opportunities for junior engineers.
Collaborative environment with cross-functional teams.
Hands-on involvement in all stages of product lifecycle.
Exposure to cutting-edge medical technology and regulatory processes.
Opportunities for continuing education and professional development.
Full Job Description
Roles & Responsibilities:
ct as technical lead for mechanical design within electromechanical medical device programs.
Own the mechanical architecture and interfaces for electro-mechanical subsystems including enclosures, mechanisms, mounts, thermal paths, cable routing, and EMI/EMC considerations.
Lead end-to-end mechanical design activities from concept, feasibility, and prototyping to design freeze and production release.
Translate user needs, system requirements, and electrical/software constraints into robust mechanical designs.
Develop and review 3D CAD models, detailed drawings, GD&T, and BOMs.
Ensure proper integration of motors, sensors, PCBs, batteries, power supplies, connectors, and cabling within mechanical assemblies.
Execute development activities in compliance with ISO 13485, FDA 21 CFR 820, ISO 14971, and applicable IEC standards.
Ensure completeness and quality of Design History File (DHF) documentation.
Lead and participate in risk management activities (dFMEA, pFMEA, hazard analysis) with cross-functional teams.
Support design changes through formal ECO/ECN processes.
Define mechanical verification strategies and support DVT, EVT, and V&V testing.
Investigate and resolve failures observed during testing, manufacturing, or field feedback.
Lead application of DFM/DFA principles for manufacturing processes.
Work closely with suppliers and contract manufacturers on tooling, materials, processes, and yield improvement.
Support FAI, PPAP, pilot builds, and design transfer to manufacturing.
Drive resolution of manufacturing issues, NCRs, and deviations related to mechanical design.
Collaborate with electronics, software, systems, quality, regulatory, and supply chain teams.
Lead and participate in design reviews, technical discussions, and customer walkthroughs.
Guide and perform engineering analyses including tolerance stack-ups (hand calculations and FEA).
Provide technical input for cost reduction, design optimization, and next-generation improvements.
Mentor and technically guide junior and mid-level engineers.
Requirements:
8+ years of experience in mechanical design and development, with significant experience in medical device NPD.
Proven experience leading mechanical development of electromechanical products through full product lifecycle in regulated environments.
Bachelor's or Master's degree in Mechanical Engineering.
Technical Skills:
Strong proficiency in CAD tools such as SolidWorks or Creo.
In-depth knowledge of materials and manufacturing processes for medical devices.
Strong understanding of electromechanical integration, thermal considerations, EMI/EMC-aware mechanical design, and reliability.
Expertise in GD&T (ASME Y14.5), tolerance stack-up, and DFM/DFA.
Knowledge of FEA and practical engineering calculations.
