Title : Document Controller
Location : Lebanon, IN
Duration : 18 month contract (potential of extension)
Overview
We’re seeking a detail‑oriented Document Controller to support controlled documentation across a
highly regulated pharmaceutical environment. You’ll manage the full document lifecycle—creation,
review / approval routing, version control, and archiving—within our electronic document management
system (EDMS), ensuring compliance with internal standards and regulatory requirements.
Key Responsibilities
- Manage, organize, and maintain controlled documents (SOPs, protocols, work instructions,
forms) within the EDMS (Veeva QualityDocs).
Ensure documents meet GMP / GxP and company compliance standards; maintain audit‑readyrecords.
Execute document revisions, updates, and version control; track changes and effective dates.Coordinate cross‑functional reviews and approvals (QA, Manufacturing, Engineering, R&D,Labs).
Monitor document status and proactively follow up to keep workflows on schedule.Support document archiving, periodic reviews, and retention requirements.Partner with internal stakeholders and contractors to standardize formats and improvedocumentation processes.
Qualifications
Experience in document control within pharma / biotech / medical device or other regulatedindustries.
Hands‑on use of an EDMS (ideally Veeva QualityDocs; MasterControl, Documentum,TrackWise, etc. also relevant).
Solid understanding of GMP / GxP and documentation compliance best practices.Strong attention to detail, organization, and follow‑through; comfortable managing highdocument volumes.
Effective communication skills and ability to collaborate with SMEs and cross‑functionalteams.
Preferred Experience
Prior coordination of review / approval workflows and change control.Familiarity with quality systems and audit support.Experience supporting documentation for manufacturing, utilities, or laboratory operations.