RemoteListed Jul 25, 2026
Commercial Labeling Project Manager (Fully Remote)
Dawar Consulting, Inc.
- Artwork-Management
- Commercial-Labeling
- Global-Labeling-Lead
- Labeling-Operations-Manager
- Labeling-Project-Manager
- Pharmaceutical-Project-Management
- Regulatory-Affairs-Project-Manager
- Regulatory-Labeling-Manager
- Regulatory-Operations
Assessed from original listing evidence
The role
Job description
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, 401KSummary: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. The ideal candidate has experience in commercial labeling, regulatory operations, artwork management, or packaging operations, along with hands-on experience using Veeva Vault or similar document management [link removed] 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.
- 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.
- Experience in GxP-regulated pharmaceutical or biotechnology environments.
- Knowledge of global commercial labeling processes.
- Experience coordinating with global stakeholders.
Originally posted on Himalayas
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