Medical Device Document Control Specialist

Actalent

Actalent is seeking a Document Control Specialist in Minneapolis, MN to manage engineering and product documentation within a regulated medical device environment. You will oversee GDP practices, maintain BOMs, and coordinate with cross-functional teams to support product releases. This contract-to-hire role focuses on quality system compliance (ISO, FDA) and requires experience with PDM/ERP systems, QMS tools, and MS Office. #J-18808-Ljbffr Actalent

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Vacancy posted 1 day ago

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