Product Development Engineer – Medical Device jobs in United States
info-icon
This job has closed.
company-logo

Ecocareers · 1 month ago

Product Development Engineer – Medical Device

Ecocareers is a company specializing in medical device innovation, and they are seeking a Product Development Engineer to lead product development for orthopedic implants and instruments. The role involves authoring test protocols, ensuring compliance with regulatory standards, and collaborating with labs and suppliers throughout the project lifecycle.

Staffing & Recruiting

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 photos videos, 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 (DVV) including benchtop, simulated use, and preclinical testing
Collaborate with manufacturing and suppliers for DFMA, process validations, and design transfer readiness

Qualification

CAD (Solid Works Creo)Orthopedic testing standardsRisk management toolsTest protocol report writingProject managementCross-functional communicationStatistical analysisMaterialsProcesses knowledgeExternal lab management

Required

Proficiency in CAD (Solid Works Creo), GDT, tolerance analysis, and fixture design
Knowledge of orthopedic testing standards (ASTM F382, F543, F1717, F2077, ISO 1424214243, etc.)
Strong capability in test protocol report 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
4–6 years of experience in Supplier Quality or Product Quality Engineering in medical device industry

Company

Ecocareers

twitter
company-logo
Ecocareers provides a specialized job search for careers that make a difference.

Funding

Current Stage
Early Stage
Company data provided by crunchbase