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Mechanical Product Validation Engineer - Only W2

Saransh Inc

Cincinnati, OH

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JOB DETAILS
SKILLS
Analysis Skills, Cross-Functional, Design Failure Mode and Effects Analysis (DFMEA), Documentation, Feasibility Analysis, Hazard Analysis, Mechanical Engineering, Medical Equipment, Problem Solving Skills, Process Failure Mode and Effects Analysis (PFMEA), Product Development, Product Engineering, Product Testing, Product/Service Launch, Quality Assurance Methodology, Research & Development (R&D), Risk Management, Root Cause Analysis, Statistics, Sterilization, Technical Presentation, Technical Writing, Test Lab, Test Plan/Schedule, Testing, Time Management, Validation Documentation, Validation Testing
LOCATION
Cincinnati, OH
POSTED
1 day ago
Role: Mechanical Product Validation Engineer
Location: Cincinnati, OH (Onsite from Day 1)
Job Type: W2 Contract

*Update from HM - We are looking for Mechanical Engineer*
*candidate needs Bachelor or Masters in Mechanical Engineering*

Must Have's:
Cleaning & Sterilization Validation, Test Method Development, product quality, DFMEA

Job summary:
  • 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.
Responsibilities:
  • 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.

About the Company

S

Saransh Inc

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