Global Labelling Associate Director, Content (Established Products)

Company: Novartis Farmacéutica
Apply for the Global Labelling Associate Director, Content (Established Products)
Location: London
Job Description:

Job Overview

#LI-Hybrid (12 days per month on-site if living within 50 miles of our London office)#LI-Remote (Homeworker if living further than 50 miles of our London office)Internal job title: Global Labelling Associate Director, Content (In-Market Brands & Global Health)Office Location: London (The Westworks), United Kingdom

We are looking for a Global Labelling Associate Director, Content (Established Products) to contribute to the development and delivery of global labelling strategies across a portfolio of products. In this role, you will support the creation of clear, consistent, and scientifically robust labelling content across development and lifecycle stages.

Responsibilities

  • Develop and maintain global labelling strategies and core labelling documents for assigned products (e.g. CDS, USPI, EU SmPC/PIL).
  • Lead and facilitate cross‑functional discussions to support alignment on labelling content and strategy.
  • Present labelling proposals and updates to governance bodies and project teams.
  • Identify emerging labelling considerations and contribute to planning, risk assessment, and mitigation strategies.
  • Analyse competitor labelling, regulatory guidance, and scientific data to inform content development.
  • Support and contribute to responses to Health Authority queries and interactions, including preparation of supporting documentation.
  • Collaborate with global and regional partners to ensure consistency and alignment across markets.
  • Mentor colleagues and contribute to audit readiness, inspections, and continuous improvement initiatives.

Essential Requirements

  • Fluency in English (written and spoken).
  • Demonstrated capability in Global Labelling and/or Global Regulatory Affairs, with a focus on labelling across development and lifecycle activities.
  • Ability to develop and maintain core labelling documents (e.g. CDS) and support major market labelling (e.g. USPI, EU SmPC/PIL) with scientific accuracy and compliance.
  • Ability to interpret clinical efficacy and safety data and translate it into clear, consistent labelling content and supporting documentation.
  • Working knowledge of global labelling standards and expectations, including major Health Authority requirements.
  • Strong collaboration and communication skills, with the ability to facilitate cross‑functional discussions and support alignment.
  • Strong planning, prioritisation, and attention to detail to deliver high‑quality work within timelines.

Commitment to Diversity and Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

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Posted: June 6th, 2026