About the role

Aplyr's Quick Take

This role is about leading the development of global labelling strategies for pharmaceutical products, focusing on creating clear and compliant labelling content. You'll work closely with various teams to ensure the labelling aligns with regulatory standards and market needs. It's primarily an individual contributor role with some mentoring responsibilities.

Good fit

Ideal candidates have extensive experience in global labelling or regulatory affairs, particularly in the pharmaceutical industry. Strong communication and collaboration skills are essential, along with a detail-oriented approach to managing complex information.

Worth noting

The position offers a hybrid work model, requiring 12 days on-site per month if living within 50 miles of the office. The role also involves significant interaction with cross-functional teams and health authorities, which may appeal to those who enjoy collaborative environments.

Job Description Summary

#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)
Office Location: London (The Westworks), United Kingdom

We are looking for a Global Labelling Associate Director, Content 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. You will work closely with cross-functional partners to ensure alignment on labelling strategy, enabling compliant and competitive product information for global markets.

Job Description

Major Accountabilities

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 paragraph

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

Skills Desired

Aplyr's read

Novartis is a Swiss-based global healthcare leader, known for its focus on innovative medicines and commitment to addressing patient needs through diverse roles.
Synthesized from recent postings & public sources

What's promising

•Novartis invests heavily in research and development, driving innovation in pharmaceuticals.
•The company offers a wide range of global career opportunities across various fields.
•Strong focus on cutting-edge therapies, including gene therapy and AI-driven solutions.

What to watch

•Regulatory challenges can impact the speed of drug approval and market entry.
•High competition in the pharmaceutical industry requires constant innovation to maintain market position.
•Complex organizational structure may slow decision-making processes.

Why Novartis

•Novartis has a robust pipeline of innovative medicines, setting it apart in the healthcare sector.
•The company emphasizes a diverse and inclusive workplace culture across its global operations.
•Novartis is a leader in digital transformation within pharmaceuticals, integrating AI and data science.

Aplyr’s read is generated by AI from public sources. Was it useful?

About Novartis

Novartis

novartis.com

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Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide. It focuses on innovative medicines, generics, and eye care.