R&D Engineer; Design Verification & Validation, Data Analysis Exp

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

Location: Tempe, AZ

Duration: 12 Months

Total Hours/Week: 40.00

Shift: 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

• 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)

• 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

• 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.