GMP Document Control Specialist
Listed on 2026-09-30
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Administrative/Clerical
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Quality Assurance - QA/QC
Kindeva Drug Delivery in the United States is seeking a document control coordinator to manage GMP documents, issue batch records and maintain the QDMS system. The role ensures compliant, timely distribution of master GMP documents and supports site transfer cases.
You will format documents to approved templates, reconcile and archive records, and serve as SME for document management processes, with occasional late-night or weekend work as needed.
Join us at Kindeva Drug Delivery as our next GMP Document Control Specialist in MO, United States.
Full responsibilities and requirements are described in the listing above.
Learn more about the GMP Document Control Specialist role in the description above.
We appreciate your interest in this position.
Join Kindeva Drug Delivery and contribute to our ongoing work.
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