Key Responsibilities:

- Responsible for Creating Labeling Strategy for the health authority interactions and handling HA or Country Organization (CO) labeling queries for assigned program/ products.
- Ensure Artwork Management for Initial Submission / Commercial Launch activities in coordination with CFT team.
- Responsible for Promotional Material Review and participate in CFT meetings representing Regulatory on strategic decisions by ensuring no misleading information.
- Responsible to Coordinate with External Vendor to ensure Translations documents are prepared / reviewed to support Global Regulatory Submissions.
- Responsible for SPL Preparation for Initial Submission / Labelling Response and Drug Listing for Approved Products as per business/agency timeline.
- Change management process of CCDS, Non-CCDS and Annual reportable labelling changes.
- Analysis of competitor information (e.g., labels,



approval packages) for regulatory policy projects and/or labelling projects
- Escalate, notify, and resolve any issues that may impact final labelling submission.
- Responsible for maintaining internal tracker for CCDS, Non-CCDS and Annual reportable labelling changes and submissions.
- Responsible for managing Global Labelling Impact Assessment (RLD update / Safety Information Update).
- Manage Labelling Team members and direct them to follow as per business process and ensure first time right quality.

Minimum Qualifications and Experience

B. Pharmacy / M. Pharmacy / B.Sc. / M.Sc. Relevant - Minimum 5 to 7 years and above of experience in Global Labelling domain.

📌 Regulatory Labeling (Bengaluru)
🏢 Biocon
📍 Bengaluru