Job Title

• Engr 2, Product Development Duration
• 12 Months Location
• Franklin Lakes New Jersey 07417

Must have: BS degree in engineering is required (Mechanical or Biomedical Engineering preferred). 2-4 years of engineering experience is required, preferably in medical devices. Demonstrated ability to utilize statistical tools and computer analysis. Ability to use Mechanical CAD tools (SolidWorks, CREO, ProE). Concept development and Fixture design using CAD Experience with sample titrations and processing samples using laboratory glassware and analytical balances General laboratory skills such as biological specimen handling and basic chemistry (i.e buffer preparation and pH adjustment) General mechanical testing equipment such as instron Technically proficient with MS OFFICE and knowledge of statistical analysis is desired. Nice to

Have:

Experience with applied biological sciences, developing bioanalytical assays and test methods Experience with handling biological specimens, particularly human clinical samples

Responsibility:

Provide solid technical skill and engineering support for design and development activities for new and existing products. Support current products in terms of quality, manufacturing, supply continuity and cost improvement. Participate in executing technical and/or cross-functional project work. Contribute to a culture of innovation by proactively generating novel concepts for new products and enhancements to current product performance. Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies. Translate customer needs into engineering requirements into specific product, packaging and process specifications. Engineer robust and manufactural products through strong understanding and application of engineering fundamentals. 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. Ensure compliance with Client quality policies, procedures and practices as well as with all local, state, federal and client's safety regulations, policies and procedures.