QA Documentation Control Specialist for Medical Devices

DEKA Research & Development in Manchester, NH, is looking for a QA Admin focusing on Document Control. This role supports the Quality Management System by managing document control processes in a medical device research environment. Responsibilities include performing document control functions, supporting the QA manager, and ensuring compliance during audits. Ideal candidates will have a Bachelor's degree, 2+ years of experience, and advanced Microsoft Office skills. Join DEKA to contribute to innovative medical solutions!
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