MERIT MEDICAL SYSTEMS, INC. 2017 Summer Internship - (Regulatory in SOUTH JORDAN, Utah

Merit Medical is looking for University students to fill our 2017 Summer Regulatory Affairs Internship program. (Preferably students in their Junior or Senior year) studying Regulatory Affairs, Engineering, Statistics, Auditing, and-or Risk Analysis. Interns will be called upon to support a variety activities in a fast paced, medical device environment. CHECK OUT REGULATORY AFFAIRS Regulatory Affairs is a unique department in a medical device company. As other departments design the device and its packaging, ensure proper testing, craft the labeling, plan production, or prepare the marketing strategy, Regulatory Affairs assembles information from all these other departments to "tell the story" to the regulating authorities for the purpose of gaining their approval to allow the device onto the market. This takes careful explanations in context of the product's intended use, its functionality, how it will be made, how it will be tested, and its risks and benefits. It also takes an understanding of the customer's needs, and requires being well-versed in the current regulatory landscape to ensure that all rules have been complied with. Regulatory Affairs is a challenging career which requires the professional to know the answers or else know where to find them. It calls for organizational skills, writing skills, and diplomacy to interact with regulating authorities in the US (primarily the US Food & Drug Administration) and in foreign markets. In many ways, Regulatory Affairs is one of the most interesting departments of the company, as it requires understanding of all other departments as well as familiarity with law, medicine, and business. SUMMARY OF JOB DUTIES Performs routine tasks involved in a Regulatory Affairs environment. ESSENTIAL FUNCTIONS PERFORMED * Write regulatory justifications and assessments. * Review and research engineering records, reports, regulations, etc. * Extracts data from various prescribed sources and processes the data following well-defined methods, and then presents the data in prescribed form. * May work on project teams to assist Regulatory Specialists and other personnel. * Performs other related duties and tasks as required. SUMMARY OF MINIMUM QUALIFICATIONS * Graduation within 2 years of a college degree. . Excellent organizational and interpersonal skills. . Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs. . Ability to work well as a team member. COMPANY HISTORY Merit Medical Systems, Inc. (NASDAQ, MMSI) was founded in 1987 by Fred P. Lampropoulos. Merit develops, manufactures and markets single-use medical devices primarily for diagnosing and treating cardiovascular and vascular disease. Merit has been successful in introducing and marketing innovative, high-quality products through its expertise in new product design and its capabilities in injection and insert molding of plastics; the application of its proprietary electronic and sensor-based technologies; and wire, extrusion and catheter technologies. The Company is utilizing its competitive advantages and technologies to develop and offer products that address a wide range of needs related to cardiology and radiology procedures performed in hospitals. Sales are made primarily to U.S. hospitals through a direct sales force. The Company markets its products in over 60 countries worldwide, utilizing a direct sales force in Europe, and distributors for the remainder of the world. MERIT MEDICAL SYSTEMS, INC.1600 West Merit Parkway (9800 South & Redwood Road)South Jordan, UT EQUAL OPPORTUNITY EMPLOYER M-F-D-V. Equal Opportunity Employer Minorities-Women-Protected Veterans-Disabled