R&D Engineer - Design Validation & Data Analysis

MillenniumSoft Inc; Tempe (AZ); On-site; USD 42,000 - 62,000; Full time

Job summary

MillenniumSoft Inc. in Tempe, AZ seeks an entry-level R&D Engineer for Design Verification & Validation with data analysis experience. This 12-month, W2 contract role offers 40 hours weekly, first shift, with pay range $20–$30/hour.

The candidate will write verification reports, develop test methods, and manage small projects while coordinating cross-functional teams to ensure quality and regulatory compliance for medical devices.

Qualifications

• Design verification/validation protocol and report writing with statistical analysis.
• Develop and coordinate test methods and validation activities.
• Project management experience, leading projects preferred.

Responsibilities

• Assist remediation to ensure EU MDR compliance for Product Engineering Surgical franchise.
• Provide engineering support for design and development of existing products.
• Participate in cross-functional teams to support quality, manufacturing, and cost improvements.
• Execute technical and cross-functional project work as directed.
• Develop and execute test methods with measurement equipment and data analysis.
• Prepare detailed reports from design verification analyses and changes.
• Present updates to stakeholders and track project plans in MS Project.
• Ensure compliance with client quality policies and safety regulations.

Skills

Design verification

Validation reports

Test method development

Project management

Education

Bachelor of Science in Mechanical Engineering

Bachelor of Science in Bioengineering

Master of Science in Mechanical Engineering

Master of Science in Bioengineering

Tools

MS Project

Statistical analysis software

Job description

MillenniumSoft Inc. in Tempe, AZ seeks an entry-level R&D Engineer for Design Verification & Validation with data analysis experience. This 12-month, W2 contract role offers 40 hours weekly, first shift, with pay range $20–$30/hour.

The candidate will write verification reports, develop test methods, and manage small projects while coordinating cross-functional teams to ensure quality and regulatory compliance for medical devices.