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Document Control Specialist 

EOE StatementWe are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
Full-Time/Part-Time Full-Time  

We're looking for someone with razor sharp attention to detail, documentation-savvy, initiative, strong work ethic, attendance reliable person to support our packaging & labelling department for animal pharmaceutical facility in Gainesville, GA. Major activities include coordination, assisting in reconciling and reviewing of paper batch packets, maintaining their training, and assisting in requesting, reviewing and revising documents.

Responsible to fill out, reconcile, and review documentation included in batch records from approved templates. Comfortable with Inventory Management using Computer Based Software to include SAP or familiarity with Oracle.

Assist in requesting, reviewing and revision documents as needed.

Familiarity with 21CFR, GDPs & GMPs

Must be able to follow precise instructions with high attention to detail and minimal oversight. Must balance priorities of several ongoing activities. Understanding of pharmaceutical GMP and GDPs is strongly preferred, due to the technical nature of the documents being managed.


Demonstrated experience coordinating documentation, ideally in a regulated manufacturing environment. Preferably experience with Viva, SAP, MS Teams, MS SharePoint, Excel, PowerPoint, and Word.

The individual must be very detail oriented and able to follow precise instructions. Understanding and familiarity of pharmaceutical documentation is strongly preferred. Must be able to create clear documentation and manage a workload of several assigned tasks.


Minimum of High School diploma or GED, plus at least 2 years of relevant experience

Location Gainesville, GA  

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