Senior Document Control Specialist - Veeva EDMS & GxP Expert

BioPhase; United States; Remote; USD 41,328 - 55,104; Full time

Job summary

A leading life sciences company is seeking a highly skilled Senior Clinical Recruiter to manage document control and formatting. This remote role requires over 5 years of experience in biopharmaceuticals, exceptional proficiency in Microsoft Word, and a strong understanding of GxP regulations. The successful candidate will oversee GxP-controlled documents and ensure compliance while supporting regulatory readiness. Join us for this indefinite contract opportunity in the U.S.

Qualifications

• 5+ years of experience in biopharmaceutical document management focused on Document Control.
• Expert-level proficiency in Microsoft Word including complex formatting.
• Strong knowledge of GxP and FDA regulations.

Responsibilities

• Manage GxP-controlled documents including creation and formatting of SOPs.
• Ensure compliance of document workflows per 21 CFR Part 11.
• Support GxP training administration.

Skills

Document Control

Microsoft Word formatting

GxP knowledge

EDMS expertise

Strong communication skills

Tools

Veeva QualityDocs

Learning Management Systems (LMS)

Job description

A leading life sciences company is seeking a highly skilled Senior Clinical Recruiter to manage document control and formatting. This remote role requires over 5 years of experience in biopharmaceuticals, exceptional proficiency in Microsoft Word, and a strong understanding of GxP regulations. The successful candidate will oversee GxP-controlled documents and ensure compliance while supporting regulatory readiness. Join us for this indefinite contract opportunity in the U.S.