Regulatory Affairs Product Lifecycle Management Associate

Overview

In this PLM regulatory role you will support global renewal and safety reporting, acting as the regulatory expert on cross-functional teams. You will coordinate submission plans with markets and ensure timely, high-quality dossiers. You’ll monitor regulatory intelligence and align with Global Regulatory, CMC, Medical, and Manufacturing functions. You help drive lifecycle maintenance for medicines, cosmetics, and medical devices, contributing to Haleon’s growth and compliance goals.

Responsibilities

• Plan and communicate regulatory submission timelines for renewals and safety reporting with stakeholders
• Monitor regulatory changes and relay their impact to relevant teams
• Collaborate with Global Regulatory (CMC, Medical, Manufacturing, Operating Units) on priorities and process requirements
• Provide regulatory support on priority projects and new product introductions with regional/local initiatives
• Deliver right-first-time dossiers and high-quality documents for submissions
• Support lifecycle management and market data requirements in renewals and safety reporting
• Act as regulatory expert within project teams to provide strategy and solutions
• Own regulatory-specific processes and improve cross-functional communication

Key requirements

• 1-3+ years of relevant regulatory experience
• BSc or relevant job-related experience
• Strong scientific background – Pharmaceutical or Life Sciences

• cross-functional collaboration
• clear communication
• problem-solving
• ownership and initiative
• Veeva Vault

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