Medical Device Associate

Roles & Responsibilities : Act independently with minimal supervision to conduct smaller approved projects. Expected to make suggestions on improvements based on recent technical knowledge. Able to contribute to cost estimating of major capital budget items and the spending of approved project funds. Contribute to the planning and execution of components of the development process, which apply to product revision or enhancement or a defined piece of a larger project. Ability to manage routine small projects without assistance. Investigate and analyze design improvement suggestions. Recommend design improvements. Perform standard engineering assignments which are typically a significant portion of a larger project. Select sound techniques to solve problems and make design recommendations under direction of supervisor. Assess results for application, validity and conformance to specifications. Recommend material and process specifications. Utilize engineering tools to solve straight forward problems (e.g., FMEA, Finite Element Analysis, Process Modeling, Design of Experiments, Mold Flow, SPC) Knowledge of the basic principles in various engineering disciplines. Must have initial training in concepts of Six Sigma quality techniques. Must know how to effectively run projects, coordinate contractors, and direct the activities of a technician Education / Experience : Minimum requirement Bachelors of Science in Engineering (discipline: Mechanical, BioEngineer, Chemical Engineer, or etc.) 1 - 3 years' experience of medical device experience Statistical background helpful Knowledge of DHF or DHF Remediation Medical Device Product Life Cycle, Design Controls Software: Microsoft Office: Word, Excel (pivot