Job Title: Documentation Specialist - Onsite, 6-Month Contract Job ID: 36218112 Location: Athens, GA Contract Duration: 6 Months Schedule: Monday to Friday, Full-Time Work Setting: Onsite Only Job Overview: Sigma Inc. is seeking a detail-oriented and tech-savvy Documentation Specialist for an onsite 6-month contract in Athens, Georgia. This role supports regulated pharmaceutical and biological development documentation processes and focuses on electronic document management systems (EDMS), records migration, and user support. Key Responsibilities:
- Act as a subject matter expert on EDMS, supporting controlled and regulatory submission documents
- Configure document templates and workflows; assist users with document creation and submission processes
- Provide routine and first-line support to internal users across development functions
- Lead migration of legacy records to current approved document management systems
- Follow precise computer system procedures with strong attention to detail and minimal supervision
- Handle multiple documentation projects simultaneously in a regulated laboratory environment
Preferred Systems & Tools:
- Veeva Vault (strongly preferred)
- Documentum, Microsoft Teams, MS SharePoint
- Familiarity with 21 CFR Part 11, GLP (FDA/EPA), GMP (FDA/EU), and VICH guidelines
- Understanding of BI policies around records, training, and information protection
Qualifications:
- Bachelor's degree + 2 years of relevant documentation experience OR
- Associate degree + 2 years of experience OR
- 4+ years of relevant professional experience in document management
The ideal candidate will have:
- Strong background in pharma or biotech documentation processes
- Excellent organizational and communication skills
- Ability to work independently, prioritize tasks, and deliver consistent, high-quality results
- Demonstrated experience working in regulated documentation environments