Remote Labeling Project Lead (Pharma/Biotech)

NEPSE Trading

United States

Remote

USD 75,768 - 84,033

Full time

14 days+

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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Paid Sick Leave
401K

Job summary

Dawar Consulting, Inc. is seeking a Labeling Project Manager for a fully remote role in the United States. You will manage end-to-end labeling workflows, coordinate artwork updates, and track project timelines in a regulated pharmaceutical environment.

Ideal candidates have 3–5+ years in pharmaceutical/biotech labeling or regulatory operations, hands-on experience with Veeva Vault, Adobe Acrobat, and GlobalVision, and strong cross-functional coordination skills.

Qualifications

  • 3–5+ years in pharmaceutical/biotech labeling or regulatory operations.
  • Experience managing commercial labeling workflows and artwork review processes.
  • Hands-on experience with Veeva Vault or similar document management/workflow systems.
  • Experience using Adobe Acrobat for proofreading.
  • Strong project coordination and organizational skills.

Responsibilities

  • Manage end-to-end commercial labeling projects from initiation to final approval.
  • Coordinate artwork review cycles, proofs, and final approvals with cross-functional teams.
  • Route and manage labeling workflows using Veeva Vault or similar systems.
  • Track project timelines, milestones, deliverables, and approval status across multiple projects.
  • Support implementation of label changes including phase-in/phase-out activities and obsolete inventory tracking.

Skills

Labeling project management
Cross-functional coordination
Project coordination
Proofreading
GxP knowledge

Tools

Veeva Vault
Adobe Acrobat
GlobalVision

Job description

Dawar Consulting, Inc. is seeking a Labeling Project Manager for a fully remote role in the United States. You will manage end-to-end labeling workflows, coordinate artwork updates, and track project timelines in a regulated pharmaceutical environment.

Ideal candidates have 3–5+ years in pharmaceutical/biotech labeling or regulatory operations, hands-on experience with Veeva Vault, Adobe Acrobat, and GlobalVision, and strong cross-functional coordination skills.

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