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R&D​/Product Development Engineer

Job in Cleveland, Cuyahoga County, Ohio, 44101, USA
Listing for: Katalyst HealthCares & Life Sciences
Full Time position
Listed on 2026-06-03
Job specializations:
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: R&D /Product Development Engineer

Roles & Responsibilities

  • Proficiency in CAD (Solid Works/Creo). GD&T tolerance analysts, and fixture design.
  • Knowledge of orthopedic testing standards (ASTM F F,

    F. F, /, etc.).
  • Strong capability in test protocol/report writing statistical analysis (/, tolerance intervals), and data integrity practices.
  • Familiarity with materials and processes:
    Ti alloys. Coctainless steel UHMWPE, PEEK. AM. coatings.
  • Understanding of design controls ISO , ISO , and regulatory pathways ((k), PMA. MDR).
  • Experience with external lab management, including protocol alignment, fixture approval, deviation handling and report review.
  • Compete in risk management tools (DFMEA EMEA) and traceability from requirement to verification
  • project management and cross functional communication, using tools like MS Project, Minitas
Education & Experience
  • Pro Client met Development experience required
  • Lead product development for orthopedic implants and instruments from concept through design transfer Author and execute test protocols and reports per ASTM/ISO 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 photos/videos, witnessing critical tests, and resolving deviations promptly.
  • Maintain design controls and risk management per ISO and CFR throughout the project lifecycle.
  • Plan and perform design verification and validation (DV&V) including benchtop. smulated use, and preclinical testing.
  • Collaborate with manufacturing and suppliers for DFMA process validations, and design transfer readiness.
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