At a Glance
- Tasks: Lead global labelling for products, ensuring accuracy and compliance across markets.
- Company: Join Novartis, a leader in the pharmaceutical industry with a commitment to inclusivity.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with diverse teams and excellent career advancement opportunities.
- Why this job: Make a real impact on global health by ensuring clear product information.
- Qualifications: Experience in Global Labelling or Regulatory Affairs and strong attention to detail.
The predicted salary is between 60000 - 80000 £ per year.
We are looking for a Global Labelling Manager, Content to support the development and delivery of high-quality global labelling for our products. In this role, you will contribute to ensuring that global product information is accurate, consistent, and compliant across markets. You will work closely with cross-functional partners to develop and maintain core labelling documents and support effective implementation across the product lifecycle.
Major Accountabilities
- 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
- 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.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Global Labelling Manager, Content (Neuroscience) employer: Meeveem Limited
At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work environment that fosters collaboration and innovation. Our London office provides a unique opportunity for employees to engage in meaningful work within the neuroscience field while enjoying flexible hybrid working arrangements. We are dedicated to employee growth, providing continuous learning opportunities and a supportive culture that values diverse perspectives, ensuring that every team member can thrive and contribute to our mission of improving patient outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Global Labelling Manager, Content (Neuroscience)
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We think you need these skills to ace Global Labelling Manager, Content (Neuroscience)
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Meeveem Limited!
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How to prepare for a job interview at Meeveem Limited
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Meeveem Limited that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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