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Mechanical Engineer – Medical Devices

Job in Caldwell, Essex County, New Jersey, 07007, USA
Listing for: Engineering-Resource-Group
Full Time position
Listed on 2026-05-21
Job specializations:
  • Engineering
    Mechanical Engineer, Product Engineer, Manufacturing Engineer, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 75000 - 95000 USD Yearly USD 75000.00 95000.00 YEAR
Job Description & How to Apply Below
Location: Caldwell

Responsibilities

  • Contract position for a Mechanical Engineer for design and development of medical devices and equipment.
  • Interprets customer specifications to define requirements for mechanical designs.
  • Applies the 3D CAD system to create mechanical design and drawings.
  • Develops detailed fabrication and assembly drawings and performs tolerance analysis.
  • Develop prototypes for design evaluation.
  • Troubleshoot and resolve design & processing issues.
  • Design documentation using electronic documentation systems.
  • Develops & execute design verification protocols and technical reports.
  • Work with internal and external resources on fabrication, inspection, and testing of new product parts and assemblies.
  • Develop & debug prototype tooling / equipment and processes.
  • Develop test methods and fixtures.
  • Train technicians and operators on new process techniques.
Qualifications
  • BS Mechanical Engineering.
  • Minimum 2 years experience with medical device design using Solid Works.
  • Experience with Design for Manufacturability and Assembly, DFM&A (cost/tooling/process considerations).
  • Experience with design and development of injection molded plastic, sheet metal, metal stampings, and machined metal components, and assemblies with high part counts highly desirable.
  • Knowledge of mechanical design and development using metric ISO/DIN dimensioning and drafting standards highly desirable.
  • Experience with a solid modeling using Solidworks and/or Pro/ENGINEER.
  • Experience in medical equipment / device design with particular experience in electromechanical, electro-pneumatic, pumping equipment. development.
  • Knowledge in medical device industry regulations and practices - ISO 13485, ISO 7198 & GMP.
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