QA Documentation Control Specialist

DEKA Research and Development is seeking a QA Admin focused on Document Control in Manchester, NH. This role supports the Quality Management System through effective document control processes in a medical device R&D environment. The qualified candidate will have a Bachelor's degree and 2+ years of experience in administering processes within a database. Strong attention to detail, excellent organizational skills, and advanced proficiency in Microsoft Word are essential for this position. DEKA offers a collaborative work environment and values innovative contributions from its team members.
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