Global Labelling Manager, Content

• 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.