Provide leadership and strategic direction for global labelling activities across a portfolio of products and projects.
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.

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.

Global Labelling Director – Content

Key skills