Document Control Specialist - Talent Groups : Job Details

We are seeking 10+ years of experience with Sr. Document Control Specialist to support Quality Control (QC) and compliance functions. This role involves managing physical and electronic GxP documentation in accordance with Good Documentation Practices (GDP) and regulatory requirements.

Key Responsibilities:

• 10+ years of experience in GxP document control within biotech, pharma, or life sciences.
• Strong knowledge of GxP, GDP, and data integrity principles.
• Must have Process and review controlled documents in an eDMS (Electronic Document Management System) or eQMS (Electronic Quality Management System) and (Veeva Quality Docs).
• Perform true copy verification reviews to ensure compliance and data integrity.
• Assist in document formatting and template standardization.