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Supplier Quality Engineer, SR. - C. R. Bard, Inc salt lake city, utah

Supplier Quality Engineer, SR. - C. R. Bard, Inc salt lake city, utah

Ad id: 1201178514215966
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C.R. BardA?s story began with one product in turn:of:the:century New York City. We now encompass the world, including the Salt Lake City, Ut, division: Bard Access Systems. In 1990, our division began as the Specialty Access Group of our sister division, Davol, Inc, in Rhode Island. After the acquisition of a small company in Salt Lake City, the group moved west, made this beautiful mountain valley home, and grew into the successful division that weA?re proud to be a part of.Our division focuses on developing, manufacturing, and distributing high:quality medical devices used by clinicians throughout the worldwide healthcare industry to access a patientA?s vasculature. Our devices assist in the delivery of chemotherapy, blood products, antibiotics, and nutrition. Responsible for managing suppliers including documentation, product and process qualification, and non:conforming product investigations. This position will support New Product Development, Manufacturing, and Regulatory to ensure systems are in compliance with all internal and external guidelines.A: Performs Supplier Audits and resulting documentation. A: Maintains documents relative to Supplier Management. A: Ownership of projects and technical Competence. A: Works independently and is Results Oriented. A: Initiates new or revised documentation and tracks through appropriate approval cycles and implementation. A: Maintains a professional working relationship with internal and external customer and support staff. A: Participates and/or leads cross:functional teams. A: Provides technical support on components, material methods, systems and equipment. A: Develops physical and functional test requirements to assure specifications and regulations are met. A: Writes, reviews and approves protocols, reports and data. A: Understands and follows company procedures and regulatory requirements. A: Participates in and provides input to training on department and division procedures, and policies. A: Analyzes problems in design, process and test development. A: Prepares and presents oral and written project updates and technical discussions. A: Develops and implements procedures to provide easy to follow instructions. The following duties and responsibilities are intended to be representative of the work performed by the incumbent(s) in this position and are not all:inclusive. The omission of a specific duty or responsibility will not preclude it from the position.A: A Bachelor degree in science or engineering with six (6) years of engineering expereince withign the medical device or equivalent regulated industry, OR Masters degree with five (5) years of engineering experience within the medical device or equivalent regulated industry. Above experience must include 3 (three) yearsA? proven and effective project management skills.Preferred qualifications include:A: Demonstrated knowledge of engineering principles through engineering experience within the medical device or equivalent regulated industry.The incumbent must demonstrate the potential ability to perform the essential functions of the job as outlined in the duties and responsibilities.Ability to make and present engineering decisionsStrong interpersonal skillsSpecific specialized engineering skills such as:Analyze and optimize existing process and ability to create new processes,Create, analyze and optimize manufacturing and quality systems,Basic tooling design and drafting knowledge,Basic product, design and prototyping, Material Science, Bioengineering principles.Ability to create and provide trainingDemonstrated comprehension of basic comparative statisticsSoftware application skillsProblem solving abilityAbility to create, review and coordinate test protocols and reportsAbility to generate engineering proposalsOral and written presentation skillsAbility to work in cross functional teamsUnderstanding of regulatory environmentThis position is in an office and laboratory environment and requires the incumbent to


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Last Updated on: December 16, 2017
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