Mechanical Product Validation Engineer

Must-Haves:

Cleaning & Sterilization Validation, Test Method Development, product quality, DFMEA

Mechanical Product Validation Engineer with hands‑on expertise in cleaning, sterilization, and reprocessing validation for reusable medical devices. Experienced in developing test methods, executing C&S feasibility and validation studies, conducting GR&R and root cause analysis, and supporting risk management and design reviews through cross‑functional collaboration.

• Develop soiling, cleaning, and extraction processes for reusable scopes and instruments, and accessories (I&A), incorporating real‑world use conditions and cleanability considerations.
• Plan, execute, and analyze Cleaning and Sterilization (C&S) feasibility studies, cleanability assessments, and sterilization validations for reusable scopes and I&A.
• Create and qualify test methods, perform Gage Repeatability & Reproducibility (GR&R) studies, and document results in engineering studies, test protocols, reports, and validation documentation, including statistical analysis as required.
• Conduct root cause analysis for C&S process issues and evaluation findings, and communicate data‑driven solutions and recommendations to R&D and cross‑functional stakeholders.
• Support development and completion of associated risk management documentation (e.g., DFMEA, PFMEA, hazard analyses) by providing hands‑on laboratory expertise and technical input.
• Support Design Reviews and Phase Exit Reviews by preparing required documentation, developing presentation materials, and presenting technical content related to cleaning, sterilization, and reprocessing.
• Partner with internal teams and external supplier resources (e.g., test laboratories, sterilization vendors) to ensure timely completion of product development and launch deliverables.