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Global Regulatory Affairs Specialist – Product Lifecycle (Mumbai & Hyderabad)

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Are you passionate about Regulatory Affairs, CMC documentation, labeling, and lifecycle management?
G&L Scientific, a globally recognized life sciences consultancy, is seeking three talented Global Regulatory Affairs Specialists to support a major regulatory transformation initiative.
This hybrid role in Mumbai or Hyderabad offers a chance to work with top-tier pharmaceutical clients, contributing directly to regulatory excellence and global compliance.


Job Overview

Position: Global Regulatory Affairs Specialist – Product Lifecycle
Company: G&L Scientific
Location: Mumbai or Hyderabad, India (Hybrid)
Employment Type: Full-time
Experience Required: Prior experience in Regulatory Affairs (CMC, labeling, lifecycle management)
Salary Range: ₹8,00,000 – ₹15,00,000 per annum (depending on experience)
Application Deadline: December 4, 2025


Key Responsibilities

  • CMC Documentation Support:
    • Compile, review, and maintain Chemistry, Manufacturing, and Controls (CMC) documents.
    • Coordinate with cross-functional teams to ensure data integrity and accuracy.
  • Labeling Activities:
    • Review and update product labeling per regulatory and internal standards.
    • Ensure alignment between approved labels and market implementation.
  • Regulatory Operations & Lifecycle Management:
    • Prepare, review, and submit regulatory filings and variations.
    • Manage renewals, maintenance submissions, and compliance updates.
    • Support digital transformation and process optimization initiatives.

Candidate Qualifications

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or Regulatory Affairs.
  • 2–6 years of relevant experience in global regulatory submissions, CMC, or labeling.
  • Excellent organizational and communication skills.
  • Detail-oriented, with the ability to manage multiple priorities in a global matrix environment.
  • Prior exposure to CHC regulatory standards preferred.

Why Join G&L Scientific?

  • Opportunity to work on global regulatory transformation projects.
  • Exposure to top-tier pharmaceutical clients and cross-functional collaboration.
  • Be part of a global team of experts driving innovation in life sciences.
  • Supportive, hybrid work environment encouraging learning and career growth.

How to Apply

Application Link

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Global Regulatory Affairs Specialist – Product Lifecycle (Mumbai & Hyderabad)
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