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New Position - R&D Engineer I
| Details |
Country: USA
Location: Minnesota-Minneapolis Plymouth, MN 55442
Total applied: 13 Job Category:Engineering
Relevant Work Experience:1+ to 2 Years
Education Level:Bachelor's Degree
Location:Plymouth, MN 55442
Status:Full Time, Employee
Occupations:Bio-Engineering;Mechanical Engineering
Career Level:Entry Level
Relevant Work Experience:1+ to 2 Years
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New Position - R&D Engineer I
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 an R&D Engineer I. This position is responsible for Conducting the design and process development of medical devices. Project engineering, prototyping, pertinent background information gathering, planning, and management of project and design teams from conception through commercial launch of medical devices. Vascular device design knowledge is a plus. Experience with catheter or device implantation is preferred. Good communication skills, verbal and written and computer proficiency required. Relocation is not available for this position. RESPONSIBILITIES: Work closely with PD, Quality, Marketing, Clinical, Regulatory and Manufacturing team members to support the successful completion of R&D project activities Assist with Product Requirements documents. Design, analyze and prototype atherectomy devices Help prepare timelines, cost analyses, and resource needs. Prepare Engineering drawings with specifications, and tolerances. Prepare Preliminary manufacturing and inspection procedures. Write Testing protocols, and reports. Transfer Technology to PD/manufacturing engineering. Cross-functional team interface. Perform job functions in accordance with applicable GMP and ISO standards. Comply with applicable FDA and international regulatory laws/standards and the ev3 Code of Conduct. Related Responsibilities: FEMCA development. Flow charts with goals or milestones. Budget tracking as needed. Concurrent engineering. Vendor identification and procurement. Assist in directing all technical efforts. Complete documentation of all project data. 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, Skills and Experience: Mechanical design of vascular devices. Catheter and/or device implant experience. BS or MS degree with 0-3 years experience, or equivalent. Degree and experience are in a field of mechanical or biomechanical engineering. Medical device development a plus (internships). Computer skills, to include spreadsheets, word processing, project, CAD etc. Knowledge of GMP and ISO regulations. Experience with statistical and analytical methods such as SPC, SQC, and DOE. Ability to manage and prioritize multiple tasks/projects with a strong problem solving ability. Strong technical writing skills. Strong interpersonal skills. Strong communication skills.
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