This candidate will be responsible for the development, implementation, maintenance, and improvement of quality assurance processes. Throughout the implementation and maintenance process, this candidate should use data analysis to better understand quality reporting measures and improve processes.ResponsibilitiesNavigating Manufacturing Instructions, Procedures and Validations to determine repetitive actions, creation of product disposition instructions and qualification reports.Assessing site documents for gaps in relation to global documentsManufacturing document redlines and updatesMaintaining listings of equipment and navigating procedures and validation documents to determine equipment documentation requirements.QualificationsBachelor's degree or equivalent in Mechanical, Electrical, or Manufacturing Engineering2 years' of industry experience in Medical DeviceStrong knowledge of quality tools used in the industryAnalytical and quantitative approach to problem solving
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