R&D Engineer (Design Verification & Validation, Data Analysis Exp is Required) - Urgent Need

Millenniumsoft, Inc

Tempe (AZ)

On-site

USD 28,000 - 41,000

Full time

14 days+

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Job summary

Millenniumsoft, Inc. in Tempe, AZ is seeking an R&D Engineer (Design Verification & Validation, Data Analysis Exp is Required) for a 12-month contract.

The role emphasizes design verification/validation, data analysis and reporting to ensure product compliance and performance. You will develop test methods, coordinate cross-functional activities, and document results with MS Project planning, supporting EU MDR remediation for medical devices.

Qualifications

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

Responsibilities

  • Assist with remediation to meet EU MDR for Product Engineering Surgical franchise.
  • Provide engineering support for design and development of existing products.
  • Lead cross-functional teams to support quality, manufacturing, and cost improvement.
  • Execute technical and cross-functional project work.
  • Develop and execute test methods with measurement equipment and data analysis.
  • Write detailed design verification reports for changes and product activities.
  • Prepare and present project updates to stakeholders.
  • Create, execute, and track project plans in MS Project and manage budgets.
  • Ensure compliance with client quality policies and safety regulations.

Skills

Design verification
Test method development
Project management

Education

BS/MS in Engineering

Job description

Position : R&D Engineer (Design Verification & Validation, Data Analysis Exp is Required)
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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