Design & Development Engineer III
Listed on 2026-08-10
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Engineering
Product Engineer, Mechanical Engineer, Manufacturing Engineer, Medical Device Industry
About Nissha Medical Technologies
Nissha Medical Technologies (NMT) is a global Contract Development and Manufacturing Organization (CDMO) where people, purpose, and technology come together to advance healthcare. Headquartered in the United States, NMT is the medical devices business unit and a wholly owned subsidiary of Nissha Co., Ltd., a publicly traded Japanese company based in Kyoto, Japan (TSE: 7915).
Job Description
About Nissha Medical Technologies
Nissha Medical Technologies (NMT) is a global Contract Development and Manufacturing Organization (CDMO) where people, purpose, and technology come together to advance healthcare. Headquartered in the United States, NMT is the medical devices business unit and a wholly owned subsidiary of Nissha Co., Ltd., a publicly traded Japanese company based in Kyoto, Japan (TSE: 7915).
Across our global organization, our teams collaborate to design and manufacture innovative medical devices and solutions that make a real difference in patients’ lives. We partner closely with our customers to solve complex challenges, move ideas forward, and support products from concept through commercialization. Our work spans patient monitoring, surgical and interventional solutions, precision components, and emerging technologies, all grounded in a strong culture of quality, accountability, and continuous improvement.
At Nissha Medical Technologies, we believe our success is driven by our people. We foster an environment where curiosity is encouraged, teamwork is valued, and individuals are empowered to grow their skills and careers. If you’re motivated by meaningful work, collaboration, and the opportunity to help shape the future of healthcare, you’ll find a place to belong at NMT.
What You Will DoNissha Medical Technologies is looking for a Design and Development Engineer III to join our Design Engineering team. The main focus of the job is to provide high level technical contribution to the design and development of product solutions based on the design inputs provided by the customer requirements. These product solutions may be systems that are mechanically or electromechanically based.
The design process utilized shall be in compliance with Quality System and standard operating procedures. In addition, this role will include responsibilities of technical oversight for the engineering team.
- Develop product specifications derived from customer requirements
- Conceptualize new product solutions that are capable of meeting customer requirements based on product specifications. These solutions may include principles of solid mechanics, fluids mechanics, thermodynamics, and thermal mechanics. These solutions may require integration of electrical and software elements provided by other team members.
- Perform engineering analysis as a means of verifying that product concepts have engineering merit and have a high likelihood of meeting the product specifications.
- Perform detailed design of product solutions including CAD Modeling, Design for Manufacturability and Assembly, Material selection, and Drawing Specifications.
- Develop detailed drawing of components and assemblies identifying critical criteria to ensure product quality.
- Identify suppliers of components and procure prototype component samples.
- Perform initial engineering builds of design prototypes.
- Perform prototype evaluations and debug samples as required.
- Develop test methods and procedures for verifying that a design meets the product specifications.
- Prepare protocols and reports of various types included as part of design verification.
- Develop procedures and instructions for assembling product designs.
- Specify or modify production processing equipment required for manufacturing the product.
- Research and develop custom manufacturing processes as required
- Design, fabricate, and verify the installation of assembly fixturing and manufacturing aids.
- Identify, document, and verify critical in-process and final acceptance product quality criteria.
- Verify and validate production equipment, processes, and test methods.
- Support and participate in the risk management process required by the medical device industry
- Support, guide, and…
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