QA Document Control Analyst - GMP/EDMS Expert
Listed on 2026-10-07
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Syngene is seeking a QA Analyst I in Baltimore to manage and archive GMP-controlled documents and support technical writing and formatting for consistency and traceability. You will ensure proper design, storage, and retrieval of papers and electronic records, working with owners and authors to maintain quality documentation.
The role requires a Bachelor’s in a scientific field and at least 3 years of cGMP QA documentation experience, plus proficiency with Microsoft Office tools.
We are currently recruiting a QA Document Control Analyst - GMP/EDMS Expert for our team in Baltimore, MD, United States.
We appreciate your interest in this position.
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This posting is for the QA Document Control Analyst - GMP/EDMS Expert role at Syngene International, based in Baltimore, MD, United States.
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