What are the responsibilities and job description for the Sterile Disposable Engineer position at Rose International?
The purpose of this contract engineering position is to support medium to large design and testing efforts pertaining to the development of new and innovative plastic sterile medical disposable products for radiology and cardiovascular devices. This role participates in the product design and development of new products and may support life cycle engineering of existing products. The individual will work as a member of a cross functional team that includes design, manufacturing, quality, regulatory, and program management in an FDA regulated environment.
Major tasks and responsibilities of position
- Lead and / or support detailed engineering design, development, and implementation of new sterile disposable product designs utilized in radiology and cardiovascular medical procedures.
- Conduct or direct testing in a Research and Development lab environment to verify concept product designs (including Samples preparation for Risk Reduction Testing, Functional Testing, etc.)
- Support verification / validation testing of production intent products using novel product designs.
- Create various design history file documentation throughout the product development process including technical assessments, test protocols / reports, and various engineering documentation.
- Writes scientific protocols, manages or performs the execution of the protocols, analyzes results, and writes reports.
- Create and modify SD designs using CAD software such as Pro Engineer and CREO. CAD models may be 3D printed as required.
- Works closely with other functions including engineering, quality, procurement, and product supply to ensure project deliverables are properly planned and aligned with broader organizational objectives.
- Other Duties as assigned.
Qualifications
