Documentation Specialist

MSI Pharma

United States

Hybrid

USD 60,000 - 80,000

Full time

14 days+

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Job summary

A global pharmaceutical company is seeking a detail-oriented professional for a document control role. In this position, you will manage controlled documents, ensure compliance, and support audits. Ideal candidates have experience in regulated environments and strong skills in MS Office, SharePoint, and Smartsheet. A bachelor's degree or equivalent experience is required. This is a remote/hybrid position based in the United States.

Qualifications

  • Experience with document control in a regulated environment.
  • Sharp attention to detail and excellent proofreading skills.
  • Organized, reliable, and able to juggle multiple priorities.

Responsibilities

  • Manage controlled documents in QMS platforms.
  • Keep records accurate, compliant, and inspection-ready.
  • Generate reports, maintain trackers, and support audits.
  • Coordinate with internal teams to keep workflows moving.

Skills

Document control
Attention to detail
MS Office
SharePoint
Smartsheet

Education

Bachelor's degree or equivalent experience

Job description

Remote / Hybrid | 🌍 Global Pharmaceutical Company

What you’ll do:
  • Manage controlled documents in QMS platforms (Veeva experience a plus)
  • Keep records accurate, compliant, and inspection-ready
  • Generate reports, maintain trackers, and support audits
  • Coordinate with internal teams to keep workflows moving
What we’re looking for:
  • Experience with document control in a regulated environment
  • Sharp attention to detail and excellent proofreading skills
  • Strong MS Office, SharePoint, Smartsheet knowledge
  • Organized, reliable, and able to juggle multiple priorities
  • Bachelor’s degree (or equivalent experience)
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