Quality Documentation Control Specialist - Compliance

DEKA Research and Development in Manchester, NH is seeking a Quality Systems Specialist to oversee documentation control processes within the medical device R&D environment. You'll be instrumental in managing Engineering Change Orders and ensuring documentation accuracy. The ideal candidate has a Bachelor's degree in a related field and 2+ years of experience with database processes. Strong proficiency in Microsoft Office and excellent organizational and communication skills are essential. Join us in creating innovative medical solutions.
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