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Salary
$110k – $122k per year
Location
Remote (likely United States)
Seniority
Middle · 3+ years exp
Employment
Contractor

Confirmed on the employer's own hiring board on Nov 5, 2026. First seen by Alion on Oct 12, 2026. Dawar Consulting scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Dawar Consulting is a staffing and professional services firm headquartered in Newark, California, in Silicon Valley, that provides contract, direct-hire and managed-services staffing alongside Workday HCM and ServiceNow implementation and support. Besides its California head office it has offices in Noida in India, Utrecht in the Netherlands and Mexico City, and its life science practice places scientists and lab staff with biotechnology and pharmaceutical clients on long-term contracts. Its openings are mostly client placements such as research associates, scientists, QC chemists, lab technicians and bioprocess engineers, plus SAP consultants and technical recruiters.

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

  • 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.

If interested, please share your updated resume at [email protected] / [email protected].

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