Quality Document Controller: ISO/QSR Compliance & Change Control
6240-AMO Manufacturing USA LLC Legal Entity
Johnson & Johnson is seeking a Document Control Specialist to support the administration, maintenance, and monitoring of QMS documentation, training records, and change control activities in compliance with FDA QSR and ISO 13485. You will coordinate document workflows, support audits, and contribute to cross-functional product launch initiatives. The role requires 2–5 years in document control or related QA functions, and familiarity with Agile/SAP systems. #J-18808-Ljbffr 6240-AMO Manufacturing USA LLC Legal Entity
Vacancy posted 2 days ago
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