Orthopedic Product Development Engineer Broadview Heights - OH - Ohio

Broadview Heights, OH, US • Posted 1 day ago • Updated 1 day ago
Contract Corp To Corp
Contract W2
12 Months
On-site
$36/hr
Fitment

Dice Job Match Score™

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Job Details

Skills

  • SolidWorks
  • GD&T
  • ASTM Testing
  • ISO 14971
  • Design Verification

Summary

****PLEASE NOTE The rates may be negotiable based on experience, education, geographic location, and other factors..****

TechnicalFunctional Skills

Proficiency in CAD (SolidWorksCreo), GD&T, tolerance analysis, and fixture design.

Knowledge of orthopedic testing standards (ASTM F382, F543, F1717, F2077, ISO , etc.).

Strong capability in test protocolreport writing, statistical analysis (9595, tolerance intervals), and data integrity practices.

Familiarity with materials and processes: Ti alloys, CoCr, stainless steel, UHMWPE, PEEK, AM, coatings.

Understanding of design controls, ISO 13485, ISO 14971, and regulatory pathways (510(k), PMA, MDR).

Experience with external lab management, including protocol alignment, fixture approval, deviation handling, and report review.

Competence in risk management tools (DFMEA, pFMEA) and traceability from requirements to verification.

Skilled in project management and cross-functional communication, using tools like MS Project, Minitab.

Prior Client Development experience required.

Roles & Responsibilities

Lead product development for orthopedic implants and instruments from concept through design transfer.

Author and execute test protocols and reports per ASTMISO standards, ensuring risk-based acceptance criteria and regulatory compliance.

Act as primary liaison with testing labs: prepare technical data packages, approve fixtures, clarify protocol details, and ensure proper sample handling and chain-of-custody.

Support lab test execution by coordinating logistics, reviewing set-up photosvideos, witnessing critical tests, and resolving deviations promptly.

Maintain design controls and risk management per ISO 14971 and 21 CFR 820 throughout the project lifecycle.

Plan and perform design verification and validation (DV&V) including benchtop, simulated use, and preclinical testing.

Collaborate with manufacturing and suppliers for DFMA, process validations, and design transfer readiness.

Education Minimum B.S. degree from an ABET-accredited school (or global equivalent) in one of the following engineering disciplines, 2-4 years of experience: Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering, Biomedical Engineering Technology, Bioengineering Technology, Aerospace Engineering or Aeronautical Engineering. Medical device, particularly the Orthopedic industry, experience preferred.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 90911958
  • Position Id: 42245
  • Posted 1 day ago
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