At a Glance
- Tasks: Lead global labelling strategies and collaborate with cross-functional teams to ensure compliance.
- Company: Join Novartis, a leader in healthcare committed to diversity and inclusion.
- Benefits: Enjoy competitive salary, professional development, and a supportive work environment.
- Other info: Flexible working options available; thrive in a dynamic and inclusive culture.
- Why this job: Make a real impact on global product information and enhance patient safety.
- Qualifications: Experience in Global Labelling or Regulatory Affairs with strong communication skills.
The predicted salary is between 80000 - 100000 € per year.
12 days per month on-site if living within 50 miles of our London office (homeworker otherwise). Office location: London (The Westworks), United Kingdom. We are looking for a Global Labelling Associate Director, Content 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
- Fluency in English (written and spoken).
- 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.
Commitment to Diversity and Inclusion / EEO
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Benefits and Rewards
Learn about all the ways we’ll help you thrive personally and professionally.
Global Labelling Associate Director, Content in London employer: Novartis UK
At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our London office provides a vibrant environment where you can thrive both personally and professionally, with flexible working arrangements and opportunities for mentorship and career growth. Join us to be part of a diverse team dedicated to making a meaningful impact in global health.
StudySmarter Expert Advice🤫
We think this is how you could land Global Labelling Associate Director, Content in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their labelling strategies and be ready to discuss how your experience aligns with their needs. Show them you’re not just another candidate!
✨Tip Number 3
Practice your pitch! Be clear about your skills and how they relate to the role of Global Labelling Associate Director. A confident and concise introduction can make a lasting impression.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re genuinely interested in joining our team at StudySmarter.
We think you need these skills to ace Global Labelling Associate Director, Content in London
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience in global labelling and regulatory affairs. We want to see how your skills align with the role, so don’t hold back on showcasing your relevant achievements!
Showcase Your Collaboration Skills:Since this role involves working closely with cross-functional teams, it’s essential to demonstrate your ability to collaborate effectively. Share examples of past experiences where you’ve successfully facilitated discussions or aligned strategies with others.
Be Clear and Concise:When writing your application, clarity is key! Use straightforward language and avoid jargon where possible. We appreciate well-structured content that gets straight to the point, especially when it comes to your labelling expertise.
Apply Through Our Website:We encourage you to submit your application through our website for a smoother process. It helps us keep track of your application and ensures you’re considered for the role. Plus, it’s super easy to do!
How to prepare for a job interview at Novartis UK
✨Know Your Labelling Stuff
Make sure you brush up on global labelling strategies and core documents like CDS, USPI, and EU SmPC/PIL. Being able to discuss these confidently will show that you understand the role and can contribute from day one.
✨Show Off Your Collaboration Skills
This role involves working closely with cross-functional teams, so be ready to share examples of how you've successfully facilitated discussions and aligned strategies in the past. Highlighting your teamwork will demonstrate you're a great fit for their culture.
✨Prepare for Health Authority Queries
Familiarise yourself with common Health Authority queries and how to respond to them. Being prepared to discuss how you would handle these interactions will set you apart as someone who understands the regulatory landscape.
✨Bring Your Analytical A-Game
Be ready to talk about how you've analysed competitor labelling and regulatory guidance in previous roles. Showing that you can interpret data and translate it into clear labelling content will prove your value in this position.
