QA Document Control Specialist; GMP & EDMS
Listed on 2026-10-11
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Quality Assurance - QA/QC
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Healthcare
Syngene International seeks a QA Analyst I to manage GMP documentation, archival and EDMS-related tasks. You will support technical writing, formatting and ensuring accuracy and consistency of controlled documents, contributing to regulatory compliance and efficient information flow across the site.
The role requires a Bachelor’s in science, 3+ years in cGMP QA documentation, and strong MS Office skills. You will work within a team to maintain document integrity and support training activities
This role, QA Document Control Specialist (GMP & EDMS) at Syngene International, could be your next opportunity.
Join us at Syngene International as our next QA Document Control Specialist (GMP & EDMS) in Baltimore, MD, United States.
We are currently recruiting a QA Document Control Specialist (GMP & EDMS) for our team in Baltimore, MD, United States.
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