Evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making minor adaptations and modifications. Improve existing manufacturing processes and act as liaison between production and engineering group in resolving problems encountered on the production floor. Assist with the introduction of new products into the Operations production area. Participates in project teams typically including one of the following: identifying and implementing process/product improvement alternatives to increase/optimize yield, efficiency, throughput, and/or performance; designing, performing, and documenting engineering test experiments to evaluate product/product performance; participating in Quality improvement activities; designing, developing, testing, and validating equipment, tools and fixtures; analyzing and interpreting process models and recommending process improvements; evaluates external process technologies; and other activities of limited scope requiring knowledge of principles and techniques commonly employed in the specific narrow area of assignments. Participate in equipment and process validation. Participate in equipment and process validation. Coordinates with the appropriate suppliers and other external resources needed in developing and implementing process/product improvement plans. Perform root cause analysis of failed product. Participates in project planning and scheduling. Perform responsibilities required by the Quality System and other duties as assigned or requested. BS Mechanical/Electrical Eng preferred with 3 + years of experience or an equivalent combination of education and work experience Experience in mechanical design and or automation preferred. Previous experience in an FDA regulated industry is a plus. Knowledge on Problem Solving / Process Improvement Methodology applied to job experience. Medical Device industry job experience preferred. Fully Bilingual (English/Spanish)