QA Document Control Specialist; GMP & EDMS
Listed on 2026-10-18
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
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
Our team is growing, and we are hiring a QA Document Control Specialist (GMP & EDMS) in Baltimore, MD, United States.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Baltimore, MD, United States.
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