Global Labelling Associate Director, Content (Established Products)
On-siteDublin, Leinster, Ireland
Job Summary
Develop and maintain global labelling strategies and content for established products across development and lifecycle activities. Lead cross-functional discussions to achieve alignment on global labelling strategy, content, and key product claims. Drive the creation and maintenance of core and major market labelling documents, presenting recommendations to governance bodies. Anticipate emerging labelling risks and develop mitigation, escalation, and contingency plans while supporting health authority interactions with evidence-based responses. Mentor colleagues and contribute to continuous improvement, inspection readiness, and knowledge sharing initiatives. This role shapes how critical product information is communicated across global markets at the intersection of science, strategy, and regulatory excellence.
Required Qualifications
- Degree in a scientific discipline
- Strong understanding of pharmaceutical development and regulatory requirements
- Experience developing and maintaining global labelling content for medicinal products across the product lifecycle
- Ability to interpret clinical efficacy and safety data and translate findings into clear labelling content
- Strong knowledge of global labelling regulations and requirements across major health authorities
- Proven ability to collaborate effectively across multidisciplinary teams and influence diverse stakeholders
- Excellent planning, prioritisation, communication, and attention to detail with a focus on quality
- Must be accessible in Dublin, Ireland
- Must not require relocation support
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