Research And Development Engineer III

** Candidates must be W2 or C2C, no 3rd party and no candidates requiring visa sponsorship. **

Develops new technology, products, materials, processes, or equipment with minimal supervision. Independently, or as a member of a team, develops, directs, and executes plans for a major segment of complex projects. Compiles and analyzes operational, test, and research data to establish technical specifications for designing or modifying products, processes and materials

• Consistently generates innovative and unique solutions to market needs and submits idea disclosures. Work is expected to result in the development of new or refined products, processes or equipmen
• Successfully completes complex engineering work in one or more of the following: technology development, product design and development, test of materials or products, preparation of specifications, process study, research investigation (animal and clinical studies), and report preparation
• Selects techniques to solve complex problems and make sound design recommendation
• Summarizes, analyzes, and draws conclusions from complex test result
• Designs and prepares complex reports to communicate results
• Designs and coordinates complex engineering tests and experiment
• Coordinates, manages, and documents project goals and progress and recommends appropriate revision
• Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment
• Interfaces with Physicians/Cath Lab personnel to obtain feedback on concepts and performance of new device
• Translates customer needs into product requirements and design specification
• Responsible for engineering documentation
• Works cooperatively with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success
• May train and/or provide work direction to technicians and entry-level engineer
• Demonstrates PDP/TPD system knowledge through delivery of high quality and high impact deliverable
• Primary work assignments will be involving supporting manufacturing line for hepatic artery infusion pump and accessories– updating engineering prints as necessary, communicating with the contract manufacturer and client operations/design teams, et

Qualification

• 5 - 8 Years with BS, 3 - 6 Years with MS, 0 - 3 Years with PhD
• CAPAs/NCEPs/SCAR investigations as needed, initiating and managing design changes,
• Experience with engineering prints and driving design changes in medical device is required
• Mechanical engineer Background
• Ability to take work direction and work independently.