Medical Device Document Control Specialist

AbbVie in Tempe, AZ is seeking a Subject Matter Expert for documentation support. You will handle document formatting, change request facilitation, and ensure alignment with regulatory requirements. Responsibilities include maintaining controlled medical-device documentation per ISO 13485 and Good Documentation Practices, ensuring approvals, revision control, distribution, and archiving. You will also review batch records for accuracy before product release. #J-18808-Ljbffr