System One
Job Title:
QA Document Control Associate Location:
Rockville, MD Shift/Schedule:
Monday–Friday, 7-4 Duration:
6-month contract, possible extension Pay Rate:
$20–$21/hour
Responsibilities
Support the Quality Assurance Document Control (QA DC) team by managing critical GMP documentation and ensuring timely, accurate processing of controlled records
Assemble, scan, and reconcile GMP batch records
Assemble and review validation binders
Create, track, and reconcile logbooks and form books
Maintain GxP paper files and perform document archiving and retrieval activities
Assist with document change requests and periodic review monitoring
Operate within the MasterControl electronic document management system (EDMS)
Collaborate with cross-functional teams across manufacturing and quality to facilitate document review and retrieval activities
Requirements
Proficiency in Microsoft Word and experience operating high-speed scanners/copiers
Familiarity with GMP documentation practices and QA document control processes
Strong organizational skills with exceptional attention to detail
Ability to manage high-volume document processing under tight timelines
Ref: #558-Scientific
#J-18808-Ljbffr
QA Document Control Associate Location:
Rockville, MD Shift/Schedule:
Monday–Friday, 7-4 Duration:
6-month contract, possible extension Pay Rate:
$20–$21/hour
Responsibilities
Support the Quality Assurance Document Control (QA DC) team by managing critical GMP documentation and ensuring timely, accurate processing of controlled records
Assemble, scan, and reconcile GMP batch records
Assemble and review validation binders
Create, track, and reconcile logbooks and form books
Maintain GxP paper files and perform document archiving and retrieval activities
Assist with document change requests and periodic review monitoring
Operate within the MasterControl electronic document management system (EDMS)
Collaborate with cross-functional teams across manufacturing and quality to facilitate document review and retrieval activities
Requirements
Proficiency in Microsoft Word and experience operating high-speed scanners/copiers
Familiarity with GMP documentation practices and QA document control processes
Strong organizational skills with exceptional attention to detail
Ability to manage high-volume document processing under tight timelines
Ref: #558-Scientific
#J-18808-Ljbffr