Description
Analog Devices is hiring a Document Control Specialist to manage document creation, revision, routing, approval, publishing, archival, and eQMS administration in a regulated medical device manufacturing environment. The role supports ISO, IATF, FDA QMSR, and ISO 13485 compliance, audit readiness, training coordination, system configuration, and stakeholder communication. It requires 1–4 years of relevant experience, knowledge of applicable quality-management requirements, strong analytical and communication skills, and a bachelor’s degree or equivalent professional experience. The position offers a $68,790–$94,605 annual wage range, a discretionary performance-based bonus, and medical, vision, dental, retirement, paid time off, and other benefits.
