TRS is seeking an experienced Document Control Coordinator to join their client's team of experienced pharmaceutical manufacturing professionals in Greenville, South Carolina!
Prepare new and revised documents such as forms, policy and procedures, and batch records in accordance with production operating systems, procedures, and quality control standards.
Ensure content accuracy and conformance to established standards.
Develop and maintain highly organized tracking and filing systems for documents, complaint files, and training records.
Create and maintain a variety of correspondence and memos.
Gather data and create complex reports including charts, graphs, tables, and spreadsheets for review and approval by internal and external customers.
Maintain all documentation for tracking purposes, filing, auditing, and correcting.
Track employee training schedule and ensure that managers have implemented necessary training in the allotted time frame.
Coordinate consumer/customer complaint program by performing tracking and performing investigations and providing written reports as requested.
Perform and report audits to internal departments.
Bachelors Degree in a science-related field
3-5 Years of experience performing document control
Strong working knowledge of Microsoft Excel
Experience within an FDA-regulated facility and with GNP controlled documents preferred
Strong organizational skills and the ability to work quickly with tight deadlines
Background Check and Drug Screen Required
We appreciate all interest in this position, however only those candidates with resumes most closely matched to the job description will be contacted to discuss a potential interview.