Labeling Project Management Contractor

2400 Broadway Avenue, CA, US • Posted 3 days ago • Updated 2 hours ago
Contract W2
On-site
$58/hr
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Documentation
  • GDP
  • Collaboration
  • Pharmaceutics
  • Supply Chain Management
  • Management
  • Workflow
  • Veeva
  • Document Management
  • Adobe Acrobat
  • Proofreading
  • Project Management
  • Organizational Skills
  • GxP
  • Communication
  • Attention To Detail
  • WebKit
  • SANS
  • Adobe CS

Summary

Job Title: Commercial Labeling Project Management Contractor

Location (Hybrid/Onsite within 50 miles of one of the following):

  • Thousand Oaks, CA (Preferred)
  • El Segundo, CA
  • Frederick, MD
  • Oceanside, CA
  • Foster City, CA

Duration: 17-Month Contract

Job Summary

We are seeking a Commercial Labeling Project Management Contractor to support commercial labeling operations in a regulated pharmaceutical/biotech environment. This role is responsible for managing end-to-end labeling workflows, artwork review cycles, documentation, and cross-functional coordination to ensure compliant and timely delivery of labeling updates.

Key Responsibilities

  • Manage end-to-end commercial labeling workflows and approvals using Veeva Vault or similar systems.
  • Coordinate artwork development, proof reviews, comment resolution, and final approvals.
  • Track project timelines, milestones, and deliverables across multiple labeling initiatives.
  • Partner with print vendors to manage artwork proofs and revisions.
  • Perform proofreading and quality checks using Adobe Acrobat and GlobalVision.
  • Support labeling changes, obsolescence tracking, and phase-in/phase-out activities.
  • Maintain compliant documentation following Good Documentation Practices (GDP).
  • Collaborate with Regulatory, Quality, Supply Chain, and global stakeholders.
  • Identify project risks, escalate issues, and provide regular status updates.

Required Qualifications

  • 3 5+ years of experience in pharmaceutical/biotech labeling, regulatory operations, or supply chain.
  • Experience managing commercial labeling workflows and artwork approval processes.
  • Hands-on experience with Veeva Vault or similar document management systems.
  • Experience using Adobe Acrobat and proofreading tools such as GlobalVision.
  • Strong project management and organizational skills.
  • Experience working in a GxP-regulated environment.
  • Excellent communication and attention to detail.

Preferred Qualifications

  • Experience with global labeling requirements.
  • Experience working with print vendors and packaging components.
  • Familiarity with Adobe Creative Suite and BarTender.

    Job Title: Commercial Labeling Project Management Contractor

    Location (Hybrid/Onsite within 50 miles of one of the following):

  • Thousand Oaks, CA (Preferred)
  • El Segundo, CA
  • Frederick, MD
  • Oceanside, CA
  • Foster City, CA
  • Duration: 17-Month Contract

    Job Summary

    We are seeking a Commercial Labeling Project Management Contractor to support commercial labeling operations in a regulated pharmaceutical/biotech environment. This role is responsible for managing end-to-end labeling workflows, artwork review cycles, documentation, and cross-functional coordination to ensure compliant and timely delivery of labeling updates.

    Key Responsibilities

  • Manage end-to-end commercial labeling workflows and approvals using Veeva Vault or similar systems.
  • Coordinate artwork development, proof reviews, comment resolution, and final approvals.
  • Track project timelines, milestones, and deliverables across multiple labeling initiatives.
  • Partner with print vendors to manage artwork proofs and revisions.
  • Perform proofreading and quality checks using Adobe Acrobat and GlobalVision.
  • Support labeling changes, obsolescence tracking, and phase-in/phase-out activities.
  • Maintain compliant documentation following Good Documentation Practices (GDP).
  • Collaborate with Regulatory, Quality, Supply Chain, and global stakeholders.
  • Identify project risks, escalate issues, and provide regular status updates.
  • Required Qualifications

  • 3 5+ years of experience in pharmaceutical/biotech labeling, regulatory operations, or supply chain.
  • Experience managing commercial labeling workflows and artwork approval processes.
  • Hands-on experience with Veeva Vault or similar document management systems.
  • Experience using Adobe Acrobat and proofreading tools such as GlobalVision.
  • Strong project management and organizational skills.
  • Experience working in a GxP-regulated environment.
  • Excellent communication and attention to detail.
  • Preferred Qualifications

  • Experience with global labeling requirements.
  • Experience working with print vendors and packaging components.
  • Familiarity with Adobe Creative Suite and BarTender.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91082005
  • Position Id: 2026-26249
  • Posted 3 days ago
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