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Mechanical Design Engineer
2 months ago
We are seeking a highly skilled Mechanical Engineer to join our team at Meso Scale Discovery. As a Mechanical Engineer, you will be responsible for designing, testing, and documenting mechanical systems for our biodefense, clinical, and life-science markets.
Key Responsibilities- Design and develop precision mechanisms and complex assemblies using machined, molded, and sheet-metal components.
- Work with cross-functional teams to support the design and development of MSD instrumentation.
- Contribute to the development of specifications for new instrumentation.
- Design, prototype, test, and troubleshoot new and existing instrumentation designs.
- Develop and execute test protocols for both informal and formal design testing.
- Design, build, and test manufacturing test fixtures to support production of new instrumentation.
- Prepare assembly and test procedures for new instrumentation designs.
- Interact with outside vendors to source parts.
- Perform design and development work in conformance with ISO and FDA cGMP processes.
- Bachelor's degree in Mechanical Engineering, Master's degree in Mechanical or Industrial Engineering, preferred.
- Minimum 5 years of relevant experience preferred.
- Medical or scientific instrument design experience preferred.
- Experience in an ISO cGMP environment preferred.
- Demonstrated CAD experience is required.
- Knowledge of the design of injection molded components desired.
- Knowledge of the design of electromechanical systems desired.
- Demonstrated understanding of GD&T tolerancing practices preferred.
- Solid understanding of manufacturing technologies including machining, molding, and sheet metal processes.
- Strong engineering fundamentals and analytical background.
- Logical problem solving and demonstrated ability to organize and move project tasks forward in an orderly and structured fashion.
- Excellent oral, written, and interpersonal communication skills.
- Solid knowledge of Solidworks, I-DEAS, Pro/Engineer, or AutoCad is preferred.
- Proficiency in MS Office suite.
- A wide degree of creativity and latitude is expected including the ability to multi-task in an environment with changing priorities.
- Demonstrated ability to develop, integrate, and validate systems in a GMP, ISO, or other regulated production environment is preferred.
- Working knowledge of the manufacture of FDA regulated devices is a plus.
This position is performed in R&D, light-manufacturing, and engineering office environments.