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Design & Test Specialist; Pro-E​/CREO

Job in Mahwah, Bergen County, New Jersey, 07495, USA
Listing for: iMPact Business Group
Full Time position
Listed on 2026-02-28
Job specializations:
  • Engineering
    Engineering Design & Technologists, Mechanical Engineer, Manufacturing Engineer, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Design & Test Specialist (Pro-E/CREO)

Our client, a Global Medical Device Manufacturer
, has an immediate opening for a Design & Test Specialist for a 12-month+ contract. Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to work with other like-minded, self-directed, and detail-oriented Top Talents in a highly collaborative and professional environment.

Assist in providing oversight to sustaining engineering teams with respect to implant and instrument design work. Assist in segments of complex multifunctional teams to advance assigned projects through continuous improvement initiatives.

Responsibilities
  • Model and detail implant and instrument designs utilizing ProE/Creo design software.
  • Demonstrate technical protocol and report writing skills.
  • Work on cross-functional design teams to address design and manufacturing changes and maintain existing designs.
  • Utilize knowledge of the surgical procedure to develop innovative solutions to solve/satisfy customer needs.
  • Support FDA and worldwide submissions through design rationales and compliance with industry standards with an international team.
  • Research legacy testing and design controls for evidence required.
  • Perform tolerance analysis
  • Draft technical memos
  • Self-starter that can understand engineering drawings, test reports, and design control documents.
Requirements
  • Bachelor's degree in a science or engineering discipline. Mechanical or Biomedical Engineering preferred.
  • 1-2+ years of product design experience in the medical device industry or other regulated industry.
  • Experienced in design controls and risk management within a regulated industry.
  • Experienced with a parametric CAD design package. Prefer ProE/Creo.
  • Expertise with Finite Element Analysis (FEA) and its application, or expertise in other scientific or engineering disciplines.
  • Demonstrated ability to effectively communicate engineering principles to all levels within the organization through oral and written means.
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