Commercial Labeling Project Manager (Fully Remote)

Dawar Consulting, Inc.; United States; À distance; USD 76 000 - 84 000; Plein temps

Avantages offerts par ce poste

Medical

Dental

Vision

Paid Sick Leave

401K

Résumé du poste

Dawar Consulting, Inc. seeks a Labeling Project Manager for a world leader in biotechnology and life sciences. This fully remote, long-term contract role offers $55-$61/hr on W2 (DOE) and a comprehensive benefits package.

You will oversee end-to-end labeling workflows, coordinate artwork updates, track timelines, and ensure compliant labeling changes in a regulated pharmaceutical environment.

Qualifications

• 3–5+ years in pharmaceutical/biotechnology labeling or related ops.
• Experience managing labeling workflows and artwork reviews.
• Proficient with Veeva Vault or similar systems.
• Proficient in Adobe Acrobat for proofreading and reviews.
• Strong project coordination and organizational skills.

Responsabilités

• Manage end-to-end labeling projects from initiation to final approval.
• Coordinate artwork reviews, proof revisions, and final approvals.
• Route and manage labeling workflows using Veeva Vault or similar systems.
• Collaborate with Regulatory, Quality, Supply Chain, Packaging, and vendors.
• Review proofs and perform proofreading using Acrobat/GlobalVision.
• Track timelines, milestones, and approvals across projects.
• Support label changes, including phase-in/phase-out activities.

Connaissances

Pharma labeling

Regulatory operations

Veeva Vault

Adobe Acrobat

Project coordination

Outils

Veeva Vault

Adobe Acrobat

GlobalVision

Description du poste

This is a remote position. Our client, a world leader in biotechnology and life sciences, is looking for a “ Labeling Project Manager (Fully Remote) ”. Rate: $55-$61/hr on W2 (DOE) Job Duration: Long-Term Contract (Possibility Of Extension) Company Benefits: Medical, Dental, Vision, Paid Sick Leave, 401K

Summary

In this role, you will be responsible for managing end-to-end labeling workflows, coordinating artwork updates, tracking project timelines, and ensuring compliant execution of labeling changes in a regulated pharmaceutical environment.

Key Responsibilities

• Manage end-to-end commercial labeling projects from initiation through final approval.
• Coordinate artwork review cycles, proof revisions, and final approvals with cross-functional teams.
• Route and manage labeling workflows using Veeva Vault or similar systems.
• Partner with Regulatory, Quality, Supply Chain, Packaging, Manufacturing, and external print vendors.
• Review artwork proofs and perform detailed proofreading using Adobe Acrobat and GlobalVision (or similar tools).
• 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.

Required Qualifications

• 3–5+ years of experience in pharmaceutical or biotechnology labeling, regulatory operations, packaging, or supply chain.
• 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 document review and proofreading.
• Strong project coordination and organizational skills.

Preferred Qualifications

• Experience in GxP-regulated pharmaceutical or biotechnology environments.
• Knowledge of global commercial labeling processes.
• Experience coordinating with global stakeholders.