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Fleet Laboratories is seeking an Associate Document Specialist – 1st Shift in Quality Assurance to perform and manage document control tasks, including procedures, batch records, analysis reports, logbooks, and notebooks. You will review documents for approval, maintain corporate records, support training record keeping, and help ensure compliance with cGMP (21 CFR Parts 11, 210 & 211).
The role emphasizes accuracy, timeliness, and collaboration with authors and owners.
Fleet Laboratories is seeking an Associate Document Specialist – 1st Shift in Quality Assurance to perform and manage document control tasks, including procedures, batch records, analysis reports, logbooks, and notebooks. You will review documents for approval, maintain corporate records, support training record keeping, and help ensure compliance with cGMP (21 CFR Parts 11, 210 & 211).
The role emphasizes accuracy, timeliness, and collaboration with authors and owners.