Position Title: Documentation Specialist
Work Location: Athens, GA 30601
Assignment Duration: 6 Months
Position Summary: Tech-savvy information management specialist to support GI Development sites / activities. Major activities include: the subject matter expert for electronic document management systems and migration of records from legacy systems.
Key Responsibilities:
Electronic Document Management (controlled documents, regulatory submission documents):
- Create and configure document templates and support site users in workflow configuration.
- Provide routine user support.
- Be the first line of user support for Development users.
- Records Migration: Support necessary transfer projects from origination location to approved document management systems.
- Must be able to follow precise computer system instructions with high attention to detail and minimal oversight.
- Must balance priorities of several ongoing activities.
Qualification & Experience:
- Demonstrated experience managing electronic document management systems, ideally in the Veeva suite of systems in a regulated laboratory environment.
- Preferably experience with Documentum, MS Teams, MS SharePoint.
- Understanding of pharmaceutical and biological development processes and documentation is strongly preferred, due to the technical nature of the documents being managed.
- Bachelor Degree + 2 years relevant experience OR Associates Degree + 2 years experience OR 4 years relevant experience.
- 21CFR Part 11, GLP (FDA and EPA), GMP (FDA and EU), VICH.
- Internal policies on Records Management, Training Management, Information Protection.
- Very detail oriented and able to follow precise instructions.