Mechanical Product Validation Engineer

Pentangle Tech Services | P5 Group

Cincinnati (OH)

On-site

USD 90,000 - 140,000

Full time

11 days ago

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

Pentangle Tech Services | P5 Group in Cincinnati, OH is seeking a Mechanical Product Validation Engineer responsible for developing and executing validation studies for reusable medical devices, focusing on cleaning, sterilization, and reprocessing validation.

The role involves creating test methods, performing GR&R and statistical analyses, supporting risk management, and collaborating with R&D, Quality, Regulatory, and external labs to ensure FDA/ISO compliance and timely product launches.

Qualifications

  • Bachelor's degree in Mechanical Engineering or equivalent.
  • 5+ years of mechanical product validation experience.
  • Hands-on validation of cleaning, sterilization and reprocessing for reusable medical devices.
  • Experience developing test methods, executing validation studies, and GR&R.

Responsibilities

  • Develop and execute validation studies for reusable medical devices.
  • Create test methods and perform GR&R, statistical analyses.
  • Investigate issues via root cause analysis and recommend corrective actions.
  • Support risk management activities including DFMEA, PFMEA, and Hazard Analysis.
  • Collaborate with R&D, Quality, Regulatory, Manufacturing, and external labs.

Skills

Root cause analysis
Statistical analysis
Cross-functional collaboration
Communication skills

Education

Bachelor's degree in Mechanical Engineering

Tools

GR&R analysis
Statistical software

Job description

We are seeking a Mechanical Product Validation Engineer with hands‑on experience in cleaning, sterilization, and reprocessing validation for reusable medical devices. The ideal candidate will support product development by developing and executing validation studies, creating test methods, performing root cause analysis, and collaborating with cross‑functional teams to ensure regulatory compliance and successful product launches.

Key Responsibilities
  • Develop soiling, cleaning, and extraction processes for reusable medical devices, including scopes, instruments, and accessories.
  • Plan, execute, and analyze Cleaning & Sterilization (C&S) feasibility studies, cleanability assessments, and sterilization validation activities.
  • Develop and qualify test methods, perform Gage Repeatability & Reproducibility (GR&R) studies, and prepare validation protocols, reports, and statistical analyses.
  • Investigate cleaning and sterilization process issues using root cause analysis and recommend corrective actions.
  • Support risk management activities, including DFMEA, PFMEA, and Hazard Analysis, by providing technical input and laboratory expertise.
  • Participate in Design Reviews and Phase Exit Reviews, preparing technical documentation and presenting validation results.
  • Collaborate with R&D, Quality, Regulatory, Manufacturing, and external testing laboratories to support product development and commercialization.
  • Ensure validation activities comply with quality standards, regulatory requirements, and project timelines.
Required Qualifications
  • Bachelor's degree in Mechanical Engineering or equivalent.
  • Minimum 5+ years of experience in mechanical product validation, preferably within the medical device industry.
  • Hands‑on experience with cleaning, sterilization, and reprocessing validation of reusable medical devices.
  • Experience developing test methods, executing validation studies, and performing GR&R.
  • Strong knowledge of root cause analysis, statistical analysis, and engineering documentation.
  • Experience supporting risk management activities, including DFMEA, PFMEA, and Hazard Analysis.
  • Strong communication and cross‑functional collaboration skills.
Preferred Qualifications
  • Experience with reusable endoscopes, surgical instruments, or similar medical devices.
  • Knowledge of medical device design controls, verification, and validation processes.
  • Experience working with external testing laboratories and sterilization service providers.
  • Familiarity with FDA and ISO standards related to reusable medical devices.
  • Strong analytical, problem-solving, and presentation skills.
Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Mechanical Product Validation Engineer
Mechanical Product Validation Engineer

Pentangle Tech Services | P5 Group • Kentucky

On-site
USD 85,000 - 120,000
Validation Engineer
Validation Engineer

Pentangle Tech Services | P5 Group • Kentucky

On-site
USD 85,000 - 125,000
Mechanical Product Validation Engineer
Mechanical Product Validation Engineer

TechDigital Group • Cincinnati (OH)

On-site
USD 80,000 - 100,000
Mechanical Product Validation Engineer
Mechanical Product Validation Engineer

Belcan Corporation • Cincinnati (OH)

On-site
USD 69,000 - 83,000
Mechanical Product Validation Engineer
Mechanical Product Validation Engineer

Belcan • Cincinnati (OH)

On-site
USD 104,000 - 125,000
Mechanical Product Validation Engineer - Johnson & Johnson
Mechanical Product Validation Engineer - Johnson & Johnson

Belcan Corporation • Cincinnati (OH)

On-site
USD 69,000 - 83,000
Medical Device Cleaning & Sterilization Validation Engineer
Medical Device Cleaning & Sterilization Validation Engineer

Belcan Corporation • Cincinnati (OH)

On-site
USD 69,000 - 83,000
Medical Device Validation Engineer – Cleaning & Sterilization
Medical Device Validation Engineer – Cleaning & Sterilization

Pentangle Tech Services | P5 Group • Kentucky

On-site
USD 85,000 - 120,000
Senior Mechanical Validation Engineer – Med Devices
Senior Mechanical Validation Engineer – Med Devices

Belcan Corporation • Cincinnati (OH)

On-site
USD 69,000 - 83,000
Cleaning Validation Engineer
Cleaning Validation Engineer

QvalFocus Inc. • Massachusetts

On-site
USD 80,000 - 100,000