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Commercial Labeling Project Manager (Fully Remote)


Job Location:

San Mateo, CA - USA

Monthly Salary: Not provided by the employer
Posted: 24 July 2026 (30+ days ago)
Application Deadline: 21 October 2026
Vacancies: 1 Vacancy

Job Summary

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. 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
  • 35 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.
If interested please share your updated resume at /.


Required Skills:

Labeling Project Management Commercial labeling Regulatory operations Veeva Vault