About the role

Aplyr's Quick Take

This role is about managing global product labeling for pharmaceuticals, ensuring accuracy and compliance across various markets. You'll be the go-to person for developing core labeling documents and facilitating discussions among cross-functional teams. It's primarily an individual contributor role with a focus on regulatory affairs and documentation.

Good fit

Ideal candidates have experience in global labeling or regulatory affairs within the pharmaceutical industry, with strong attention to detail and the ability to collaborate across teams. A background in interpreting clinical data and a few years of relevant experience would be beneficial.

Worth noting

The position offers a hybrid work model, requiring 12 days on-site per month if you're within 50 miles of the London office. The role emphasizes continuous improvement and audit readiness, which may appeal to those who enjoy process optimization.

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 Manager, Content to support the development and delivery of high-quality global labelling for our products.

In this role, you will contribute to ensuring that global product information is accurate, consistent, and compliant across markets. You will work closely with cross-functional partners to develop and maintain core labelling documents and support effective implementation across the product lifecycle.

Job Description

Major Accountabilities

Act as labelling lead for assigned products, developing and maintaining global core labelling documents and major market labels (e.g. CDS, USPI, EU SmPC/PIL).
Organise and facilitate cross-functional labelling discussions (e.g. ELTF meetings) to support alignment on content.
Collaborate with Global Labelling colleagues and cross-functional teams to ensure consistent, compliant, and competitive labelling content.
Conduct research across competitor labels, regulatory guidance, and clinical data to inform labelling updates.
Prepare documentation to support labelling changes and contribute to responses to Health Authority queries.
Support timely implementation of labelling updates across countries, ensuring alignment with global standards.
Maintain high-quality documentation, including version control, references, and rationale for changes.
Support audit and inspection readiness, mentoring colleagues where appropriate, and contributing to continuous improvement initiatives.

Essential Requirements

Fluency in English (written and spoken).
Demonstrated capability in Global Labelling, Regulatory Affairs, or a related pharmaceutical discipline.
Working knowledge of core labelling concepts and major market formats (e.g. CDS, USPI, EU SmPC/PIL).
Ability to interpret clinical and safety data and translate it into clear, consistent labelling content.
Strong attention to detail, with the ability to maintain accurate documentation and traceability.
Ability to collaborate effectively across cross-functional teams and manage competing priorities.

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.