Commercial Labeling Project Manager (Fully Remote)

๐Ÿข Dawar Consulting, Inc. ยท all Dawar Consulting, Inc. jobs
๐Ÿ“ United States
๐Ÿ“… Posted 2026-07-25 ยท via Himalayas
๐Ÿท Labeling-Project-Manager,Commercial-Labeling,Regulatory-Operations,Artwork-Management,Pharmaceutical-Project-Management,Regulatory-Labeling-Manager,Labeling-Operations-Manager,Global-Labeling-Lead,Regulatory-Affairs-Project-Manager
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This is a remote position.
Our client, a world leader in biotechnology and life sciences, is looking for a โ€œ Labeling Project Manager (Fully Remote) โ€.
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. 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 systems. 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
- 3โ€“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.

โ€‹If interested, please share your updated resume at /.

Originally posted on Himalayas

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