Global Labelling Director – Content

Novartis

Global Labelling Director leading global labelling strategies in the pharmaceutical industry. Responsible for high-quality labelling content aligned with product strategies.

Posted 7/21/2026full-timeLondon • 🇬🇧 United KingdomSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in global labelling strategies and regulatory affairs within the pharmaceutical or life sciences industry, with a strong focus on developing high-quality labelling content that meets regulatory requirements and aligns with product development stages.

Highest-signal resume keywords

Global Labelling ExperienceRegulatory Affairs KnowledgePeople Management SkillsCross-Functional CollaborationStrong Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Labelling Strategy DevelopmentRegulatory DocumentationClinical Data AnalysisSafety Information InterpretationLabelling Content Creation

Soft Skills

Team LeadershipInfluencing Decision-MakingPriority Management

Tools & Technologies

Labelling ToolsRegulatory Compliance Systems

Industry Keywords

Pharmaceutical IndustryLife Sciences IndustryGlobal Labelling FrameworksRegulatory RequirementsMatrix Environments

About the role

Key responsibilities & impact

Lead, develop and support a team of labelling professionals, fostering an inclusive and high‑performing environment.
Define and deliver global labelling strategies aligned with target product profiles and overall asset plans.
Oversee the development and maintenance of core and major market labelling documents.
Provide guidance on interactions with regulatory authorities, including labelling discussions where applicable.
Collaborate with cross‑functional partners to ensure alignment on labelling strategy and execution.
Ensure labelling content reflects current regulatory requirements, scientific evidence, and competitive insights.
Support the development of evidence packages and regulatory documentation.
Drive continuous improvement in labelling processes, tools, and ways of working.

Requirements

What you’ll need

Experience in global labelling and/or regulatory affairs within the pharmaceutical or life sciences industry.
Demonstrated ability to develop and deliver labelling strategies across product development and lifecycle stages.
Strong understanding of clinical data, safety information, and regulatory requirements, with the ability to translate these into clear labelling content.
Knowledge of global labelling frameworks and expectations across major markets.
Experience working in cross‑functional, matrix environments with multiple stakeholders.
Proven people management experience, including leading, developing and supporting individuals or teams in a professional setting.
Strong communication skills, with the ability to present complex information clearly and influence decision‑making.
Ability to manage priorities effectively and deliver high‑quality outcomes within timelines.

Benefits

Comp & perks

#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)