Document Control Analyst Medical Devices & Compliance

Analog Devices, Inc. in Wilmington, MA, is seeking a professional-level Document Control specialist to manage the document lifecycle within a regulated medical device manufacturing environment. You will apply QMS/eQMS knowledge to ensure audit readiness, training support, system integrity, and compliant results. Responsibilities include creating, revising, routing, approving, publishing, and archiving documents in the eQMS; reviewing for completeness and compliance; administering user accounts; #J-18808-Ljbffr