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Covidien is a leading global healthcare products company that creates innovative medical solutions for better patient outcomes & delivers value through clinical leadership & excellence. We deliver outstanding results & innovative solutions in the Medical Device & Medical Supplies segments. Through progressive thinking & cutting-edge technologies, Covidien is well positioned to lead the way in today's rapidly changing healthcare industry. Whatever your specialty or ambitions, you can make a difference at Covidien - both in the lives of others & your career. At Covidien, we strive to fully understand our marketplace, customers, communities & employees, & we enter into relationships with a sense of honesty, fairness & trust. We are an affirmative action/equal opportunity employer.
Ensure that supplier non-conformance events are closed with a sense of urgency, in a timely fashion, and minimal disruption to manufacturing. Perform qualifications to support changes to existing components or new components and materials - 10% Assist with the qualification of new suppliers, new components, and changes by developing and executing, in conjunction with other internal groups, a robust and complete set of plans and requirements for such qualifications. Interfaces with External Suppliers -30% Maintain a professional, ethical, and credible image with suppliers and internal functions, ensuring that this position is deemed a resource person to Sourcing, Manufacturing, and External Suppliers. In conjunction with Sourcing, initiate supply chain based improvements such as Dock to Stock, cost improvements and consolidation projects. Conduct supplier visits per audit schedule, as needed, and in support of issue resolution with detailed reports and agreed actions in conjunction with the supplier and other internal groups. Requirements: Any combination equivalent to, but not limited to, the following: Education/Training/Experience: Bachelor of Science degree in engineering, physical life sciences, or related technical field with 0 to 3 years experience in quality in the medical device industry or 0-2 years experience with an applicable MS degree. ASQ certification or equivalent preferred Knowledge/Skills/Abilities: Knowledge of basic quality tools, risk analysis, statistics, design of experiment Basic reading and math Reading drawings Computer literate; use of word processing, spreadsheets Quality System Requirements ISO procedures / FDA requirements Medical Device Directives (MDD) Use of various tools, including microscopes, calipers, and other inspection equipment Recognize problems and take corrective measures Excellent written and verbal communication skills Self-motivated and committed to a team approach Physical Requirements Typically requires close visual attention to work being performed and considerable sitting for long periods of time with occasional stooping, bending, reaching, standing, grasping, feeling, etc. May require occasional lifting, carrying, pushing, pulling, or to otherwise move objects of up to, but not limited to, 20 lbs. Frequent repetitive motion tasks performed.