At a Glance
- Tasks: Lead global labelling strategies and collaborate with cross-functional teams for product compliance.
- Company: Join Novartis, a leader in healthcare innovation and inclusivity.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with mentorship opportunities and a focus on continuous improvement.
- Why this job: Make a real impact on global health through clear and compliant labelling.
- Qualifications: Experience in Global Labelling or Regulatory Affairs with strong communication skills.
The predicted salary is between 80000 - 100000 £ per year.
We are looking for a Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism) to contribute to the development and delivery of global labelling strategies across a portfolio of products. In this role, you will support the creation of clear, consistent, and scientifically robust labelling content across development and lifecycle stages. You will work closely with cross-functional partners to ensure alignment on labelling strategy, enabling compliant and competitive product information for global markets.
Major Accountabilities
- Develop and maintain global labelling strategies and core labelling documents for assigned products (e.g. CDS, USPI, EU SmPC/PIL).
- Lead and facilitate cross-functional discussions to support alignment on labelling content and strategy.
- Present labelling proposals and updates to governance bodies and project teams.
- Identify emerging labelling considerations and contribute to planning, risk assessment, and mitigation strategies.
- Analyse competitor labelling, regulatory guidance, and scientific data to inform content development.
- Support and contribute to responses to Health Authority queries and interactions, including preparation of supporting documentation.
- Collaborate with global and regional partners to ensure consistency and alignment across markets.
- Mentor colleagues and contribute to audit readiness, inspections, and continuous improvement initiatives.
Essential Requirements
- Demonstrated capability in Global Labelling and/or Global Regulatory Affairs, with a focus on labelling across development and lifecycle activities.
- Ability to develop and maintain core labelling documents (e.g. CDS) and support major market labelling (e.g. USPI, EU SmPC/PIL) with scientific accuracy and compliance.
- Ability to interpret clinical efficacy and safety data and translate it into clear, consistent labelling content and supporting documentation.
- Working knowledge of global labelling standards and expectations, including major Health Authority requirements.
- Strong collaboration and communication skills, with the ability to facilitate cross-functional discussions and support alignment.
- Strong planning, prioritisation, and attention to detail to deliver high-quality work within timelines.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Global Labelling Associate Director London employer: Meeveem Limited
At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work culture that fosters collaboration and innovation. Our London office provides a hybrid working model, allowing flexibility for employees while ensuring they are part of a supportive team dedicated to advancing global labelling strategies in the healthcare sector. With ample opportunities for professional growth and development, Novartis is committed to empowering its employees to make a meaningful impact in the lives of patients worldwide.
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We think you need these skills to ace Global Labelling Associate Director London
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