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R&D Engineer (Must Have Design Verification/Validation, Test Method, Projext Mgmt Exp)

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Onsite

R&D Engineer (Must Have Design Verification/Validation, Test Method, Projext Mgmt Exp)

MillenniumSoft Inc

R&D Engineer (Must Have Design Verification/Validation, Test Method, Projext Mgmt Exp)

Skills

RData AnalysisCompliance

2 months ago

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Important information


Contract type:

Freelance / Contract

Location:

Tempe, AZ, USA

Work mode:

Onsite

Published on:

23 August 2026

What they need


Position : R&D Engineer Location : Tempe, AZ Duration : 12 Months **Total Hours/week : 40.00

pay rate-$20-30/hr** 1st Shift Client: Medical Device Company Job Category: Engineering Level of Experience: Entry Level Employment Type: Contract on W2 (Need US Citizens or GC Holders Only) Work hours: M-F 8:00a - 5:00p

3 Must Haves On The Resume

  • Design verification/validation protocol and report writing (including statistical data analysis using statistical analysis software)
  • Develop and coordinate test method and design validation/verification activities
  • Project management experience (lead projects preferred)

Education Requirements

  • Bachelor of Science in Engineering (Mechanical or Bioengineering preferred) with minimum 3 - 4 years of professional experience or Master of Science (Mechanical or Bioengineering preferred) with minimum 2 years professional experience

Job Description

  • Assist with the remediation process of existing products in efforts to bring the product lines in compliance with the EU MDR regulations for the Product Engineering Surgical franchise.
  • Provide solid technical skill and engineering support for design and development activities for existing products.
  • Participates and/or leads cross-functional teams. Support current products in terms of quality, manufacturing, supply continuity and cost improvement.
  • Participate in executing technical and/or cross-functional project work.
  • Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis.
  • Write detailed technical reports based on design verification analysis/testing for design changes and product design activities.
  • Prepares and presents oral and written project updates and technical discussions to relevant stakeholders.
  • Creates, executes, and tracks project plans in MS Project to completion while maintaining the overall project budget.
  • Ensure compliance with client quality policies, procedures, and practices as well as with all local, state, federal and client safety regulations, policies and procedures.
  • BS degree in engineering is required (Mechanical or Biomedical Engineering preferred) with a minimum of 4 years of engineering experience is required, preferably in medical devices or master’s degree (Mechanical or Biomedical Engineering preferred) with a minimum of three years of engineering experience.
  • Demonstrated ability to utilize MS Project, statistical tools, and computer analysis.

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