Mechanical Product Validation Engineer Only W2

Saransh Inc

Job Location:

Cincinnati, OH - USA

Monthly Salary: Not Disclosed

Posted on: 23 days ago

Vacancies: 1 Vacancy

Job Summary

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 Haves:
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.

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 Haves: Cleaning & Sterilization Validation Test Method Devel...

Role: Mechanical Product Validation Engineer
Location: Cincinnati OH (Onsite from Day 1)

Job Type: W2 Contract

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.