Manufacturing Engineer

At ev3 we’re committed to developing innovative endovascular technologies for coronary, peripheral and neurological applications. Creative, competent people with a passion for enhancing healthcare around the globe have driven our success. Join us as we grow by making a meaningful difference.    We are currently seeking a Manufacturing Engineer.  This position is responsible for Supporting the manufacturing of ev3 products to ensure Operations core metrics are successfully achieved. Providing technical leadership and support of manufacturing improvements and floor support for assigned product lines. RESPONSIBILITIES · Develops and maintains the documentation necessary to ensure the consistent manufacture of ev3 products (processes, drawings, and shop floor paperwork). · Provides engineering support for troubleshooting efforts for any process issues in designated area. Summarize and draw conclusions from test results leading to effective technical resolution of process problems. · Works with Process Development engineers to ensure design for manufacturing elements are incorporated into PDP activities. · Identifies, justifies, and implements significant data driven projects to reduce manufacturing costs, improve processes, increase product reliability, and enhance process capability. · Designs and evaluates new and existing fixtures and equipment, test methods, specifications, layouts, and standards supporting a Lean manufacturing environment. · Identify and recommend manufacturing technologies to strategically develop business objectives and potential opportunities. · May have supervisory responsibility for technician staff. · Comply with applicable FDA and international regulatory laws/standards and the ev3 Code of Conduct. · Other duties as assigned or required This position is located at our manufacturing facility in Plymouth, MN.     We offer competitive compensation, generous benefits, and the opportunity to improve the lives of people everywhere. For consideration, please apply online at www.ev3.net. No phone calls please. Equal Opportunity Employer/ Affirmative Action Employer.

MINIMUM QUALIFICATIONS: Education:  BS or MS degree (Engineering, Manufacturing, or other technical field)   Experience:  · 3 to 5 years of relevant experience, preferably in a medical device industry · Experience with design and process FMECA, Process Validation and variability reduction applications. · Experience with medical device based products and processing and technologies. · Implementation and support of Lean Manufacturing, Demand Flow, Total Quality tools. · Application of statistical and analytical methods such as SPC, SQC, and DOE. · Process background (development, capability, optimization, validation) within a regulated industry. · Development of manufacturing documentation (MP, IP, BOM) · Development and qualification of tooling/equipment (IQ/OQ/PQ, support, design) · Participation on project teams tasked with new process/product development and the successful transfer into manufacturing. · Manufacturing continuous improvement support. · Test protocol generation, execution, and reporting.Job Code : 772 Division/Department : CARDI Travel Required : None