Skip to main content
Posted 21 May, 2026

Assistant Manager, Labeling Reviewer

Amneal Pharmaceuticals
Ahmedabad City, Gujarat, India Full Time
Reference: 218_756524_7699

Required Skills:

  • Strong knowledge of country specific regulatory labeling requirements
  • Understanding of packaging materials and artwork processes
  • Familiarity with labeling software/tools
  • Attention to detail
  • Strong coordination and communication skills
  • Time management and ability to handle multiple projects

Preferred Skills:

  • Experience in International Labeling (India, EU, Canada, and ROW markets)
  • Exposure to digital labeling systems / automation tools
  • Knowledge of pharmacovigilance-related labeling updates

Key Responsibilities:

  • Define and execute labeling strategies for India, EU, Canada, and ROW markets.

  • Ensure alignment of local labeling with Core Data Sheet (CDS) / Company Core Safety Information (CCSI).

  • Drive harmonization of labeling content across regions while addressing country-specific requirements.

  • Review labeling content as per regulatory requirements for India, EU, Canada, and ROW (Asia, Africa, MENA, CIS, LATAM) markets.

  • Ensure labeling content aligns with approved dossiers, SmPC, PI, or local regulatory approvals.

  • Maintain consistency in labeling format, terminology, and design templates across markets.

  • Ensure compliance with:

  • CDSCO regulations and labeling requirements
  • EU Guidelines (EMA, QRD templates)
  • Health Canada labeling requirements
  • Country-specific regulations for ROW markets (Asia, Africa, LATAM, MENA, CIS)
  • Artwork Management

    • Review and verify artwork for technical accuracy, regulatory compliance, and readability.
    • Manage lifecycle of artwork from initiation to final approval and implementation.
    • Ensure version control and archival of approved artworks.
  • Regulatory Compliance & Review

    • Perform detailed review of labeling components against:
      • Approved regulatory submissions
      • Country-specific labeling regulations
      • Internal SOPs and guidelines
    • Identify gaps and ensure timely implementation of regulatory updates and variations.
    • Support responses to regulatory queries related to labeling.
  • Documentation & Systems

    • Maintain labeling documentation, templates, and checklists.
    • Ensure compliance with data integrity and documentation practices.
    • Support implementation and continuous improvement of labeling systems and processes.
  • Process Improvement

    • Contribute to standardization and harmonization of labeling processes across regions.
    • Support global initiatives for Artwork Management Systems (AMS) and labeling tools.
    • Track KPIs such as cycle time, right-first-time approvals, and compliance metrics.
  • Team Leadership & Capability Building

    • Lead and manage a team of international labeling professionals.

    • Provide technical guidance on complex labeling requirements.

    • Drive training programs on global labeling regulations and systems.

  • Cross-functional Collaboration

    • Collaborate with:

      • Global Regulatory Affairs (submissions teams)

      • Pharmacovigilance (for safety updates)

      • Quality Assurance

      • Packaging & Artwork teams

      • Supply Chain

      • Support global product launches, renewals, and variations.

      • Digital Systems & Innovation

  • Lead implementation and optimization of labeling systems:

    • Artwork Management Systems (AMS)

    • Labeling content management tools

  • Drive digital initiatives (e.g., labeling intelligence, automation programs like ALI).

  • Ensure data integrity, compliance, and system efficiency.

Master Degree

Sign up for Job Alerts