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.
Responsibilities
Navigating 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 documents
Manufacturing document redlines and updates
Maintaining listings of equipment and navigating procedures and validation documents to determine equipment documentation requirements.
Qualifications
Bachelor's degree or equivalent in Mechanical, Electrical, or Manufacturing Engineering
2 years' of industry experience in Medical Device
Strong knowledge of quality tools used in the industry
Analytical and quantitative approach to problem solving
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