R&D Engineer

Client: Medical Device Company pay rate-$20-30/hr Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) Work hours: M-F 8:00a - 5:00p Hybrid - 3 days minimum onsite Possible Temp To Hire How much travel and where will they be travelling? Puerto Rico if necessary (no more than 25%) 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 Position: R&D Engineer Location : Tempe, AZ Duration : 8+ Months contract Client: Medical Device Company pay rate-$20-30/hr Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) Work hours: M-F 8:00a - 5:00p Hybrid - 3 days minimum onsite Possible Temp To Hire How much travel and where will they be travelling? Puerto Rico if necessary (no more than 25%) 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 Masters 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 BD quality policies, procedures and practices as well as with all local, state, federal and BD 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 minimum of three years of engineering experience. Demonstrated ability to utilize MS Project, statistical tools and computer analysis. #J-18808-Ljbffr