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 F382 F543, F1717, F2077, 150, 14242/14243, etc.).
• Strong capability in test protocol/report writing statistical analysis (95/95, tolerance intervals), and data integrity practices.
• Familiarity with materials and processes:
  Ti alloys, Coctainless 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.
• Experience in risk management tools (DFMEA, EMEA) and traceability from requirement to verification.
• Project management and cross‑functional communication, using tools like MS Project, Minitas.

• 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 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.

Entry level

Contract

Pharmaceutical Manufacturing