Teams at DAWAR CONSULTING INC

Manage end-to-end commercial labeling projects in a regulated pharmaceutical environment: coordinate artwork review cycles, route workflows in Veeva Vault, proofread artwork, track timelines and approvals, partner with regulatory/quality/supply chain/packaging/manufacturing and external vendors, and support label implementation including phase-in/phase-out and obsolete inventory tracking.

Coordinate global clinical labeling implementation, map and validate label content in Bartender, partner with Regulatory Affairs and quality teams, author SOPs and process improvements, and support labeling updates to ensure compliance with FDA, cGMP, and company requirements.

Conduct and design complex laboratory experiments supporting gene therapy projects. Execute bench work, analyze data, prepare technical reports and protocols, maintain GMP/GLP-compliant documentation, troubleshoot, and contribute as an expert team member or principal investigator.