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Intellectt, Inc

Mechanical Engineer - NPD

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What they do

A Mechanical Engineer researches, designs, develops, constructs, and tests mechanical devices including machines, engines and tools. Works on devices ranging from power generators to household dishwashers to surgical equipment. May specialize in a particular type of machine or tool. May develop new devices or improve existing ones to run more efficiently.

$119,345 / year median in California

+0% projected growth

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Job Description

Mechanical Engineer - NPD at Intellectt, Inc Mechanical Engineer - NPD at Intellectt, Inc in Castro Valley, California Posted in about 2 hours ago.

Type:

full-time

Title :

Mechanical Engineer -

NPD Location:
Dublin, CA Work Arrangement:
Onsite Experience:

8-12 Years Job Description We are seeking an experienced Mechanical Engineer - NPD to provide technical leadership for mechanical design and development within electromechanical medical device programs. The ideal candidate will have strong experience taking products from concept and prototyping through validation, production release, and design transfer in a regulated medical-device environment. Key Responsibilities Serve as a Technical Lead for Mechanical Design within electromechanical medical device programs. Own mechanical architecture and interfaces for enclosures, mechanisms, mounts, thermal paths, cable routing, and EMI/EMC considerations . Lead end-to-end mechanical design activities from concept, feasibility, and prototyping through 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 . Integrate motors, sensors, PCBs, batteries, power supplies, connectors, and cabling into mechanical assemblies. Ensure compliance with applicable medical-device standards and regulations, including

ISO 13485, FDA 21 CFR 820, ISO

14971, and relevant IEC standards . Maintain completeness of Design History File (DHF) documentation. Lead and participate in dFMEA, pFMEA, and hazard analysis . Support design changes through ECO/ECN processes . Define mechanical verification strategies and support EVT, DVT, and V&V testing . Investigate and resolve mechanical failures identified during testing, manufacturing, and field feedback. Lead implementation of DFM/DFA principles. Work with suppliers and contract manufacturers on tooling, materials, manufacturing processes, and yield improvement . Support FAI, PPAP, pilot builds, and design transfer to manufacturing . Drive resolution of manufacturing issues, NCRs, and deviations . Collaborate closely with Electronics, Software, Systems, Quality, Regulatory, and Supply Chain teams . Lead design reviews, technical discussions, and customer walkthroughs. Perform engineering analyses including tolerance stack-ups, hand calculations, and FEA . Provide technical input for cost reduction, design optimization, and next-generation product improvements . Mentor and technically guide junior and mid-level engineers. Required Experience 8-12 years of Mechanical Design & Development experience. Significant experience in Medical Device New Product Development (NPD) . Proven experience leading electromechanical product development through the full product lifecycle in a regulated environment. Experience taking products from concept ? prototype ? validation ? production . Required Technical Skills SolidWorks or Creo Medical-device materials and manufacturing processes Electromechanical integration Thermal considerations EMI/EMC-aware mechanical design Reliability engineering

GD&T - ASME Y14.5

Tolerance stack-up DFM/DFA FEA and engineering calculations PLM/QMS systems such as Windchill or Agile Medical-device development and regulated product lifecycle processes Regulatory & Quality Experience Strong understanding of:

ISO 13485 FDA 21 CFR 820 ISO 14971

Design History File ( DHF ) dFMEA / pFMEA Hazard analysis ECO/ECN Design verification and validation

EVT / DVT / V&V

Design transfer and production release NCRs and deviations Preferred Qualifications Experience with Windchill or Agile PLM/QMS . EMI/EMC-aware mechanical design experience. Thermal management experience. Supplier and contract manufacturer management. Experience with FAI, PPAP, and pilot builds . Experience supporting tooling and manufacturing processes. Strong understanding of cost reduction and design optimization. Experience conducting design reviews and technical presentations. Experience mentoring junior and mid-level engineers. Experience integrating motors, sensors, PCBs, batteries, power supplies, connectors, and cable routing . Education Bachelor's or Master's degree in Mechanical Engineering or a related engineering discipline. Ideal Candidate Profile The ideal candidate will have: 8+ years of mechanical design and development experience Strong medical-device NPD background Hands-on SolidWorks or Creo experience Strong mechanical architecture and electromechanical integration skills Expertise in

GD&T, ASME

Y14.5, and tolerance stack-ups Strong DFM/DFA and FEA experience Experience with

ISO 13485, FDA 21 CFR

820, and

ISO 14971

Experience with DHF, FMEA, EVT/DVT, and V&V Experience supporting design transfer, pilot builds, FAI/PPAP, and production release Strong cross-functional technical leadership experience