At a Glance
- Tasks: Lead global labelling strategies and collaborate with cross-functional teams to ensure compliance.
- Company: Join Novartis, a diverse and inclusive employer dedicated to improving lives.
- Benefits: Flexible working options, competitive salary, and opportunities for personal and professional growth.
- Other info: Be part of a supportive community that values diversity and innovation.
- Why this job: Make a real impact in healthcare by developing clear and robust labelling content.
- Qualifications: Experience in Global Labelling or Regulatory Affairs and strong communication skills.
The predicted salary is between 70000 - 90000 £ per year.
We are looking for a Global Labelling Associate Director, Content (Established Products) 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.
About the Role
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.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?
Global Labelling Associate Director, Content (Established Products) employer: Novartis
Novartis is an exceptional employer that fosters an inclusive and collaborative work culture, making it a great place for professionals seeking meaningful careers in the pharmaceutical industry. With opportunities for personal and professional growth, employees benefit from a supportive environment that values diversity and encourages innovation. Located in London, the company offers a hybrid working model, allowing flexibility while being part of a community dedicated to improving patient lives.
StudySmarter Expert Advice🤫
We think this is how you could land Global Labelling Associate Director, Content (Established Products)
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Novartis on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Research Novartis' recent projects and their approach to global labelling. This shows you're genuinely interested and ready to contribute from day one.
✨Tip Number 3
Practice makes perfect! Get a friend to do a mock interview with you. Focus on articulating your experience in global labelling and how it aligns with Novartis' goals. Confidence is key!
✨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 serious about joining the Novartis team.
We think you need these skills to ace Global Labelling Associate Director, Content (Established Products)
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Global Labelling Associate Director role. Highlight your experience in global labelling and regulatory affairs, and show how your skills align with the job description. We want to see how you can contribute to our team!
Showcase Your Collaboration Skills:Since this role involves working closely with cross-functional partners, emphasise your collaboration and communication skills. Share examples of how you've successfully facilitated discussions or aligned teams in previous roles. We love a team player!
Be Clear and Concise:When writing your application, keep it clear and to the point. Use straightforward language to convey your experience and achievements. We appreciate well-structured applications that are easy to read and understand.
Apply Through Our Website:Don’t forget to submit your application through our official website! This ensures that your application is reviewed properly and gives us all the info we need to consider you for the role. We can’t wait to hear from you!
How to prepare for a job interview at Novartis
✨Know Your Labelling Stuff
Make sure you brush up on global labelling strategies and core documents like CDS and USPI. Being able to discuss these confidently will show that you understand the role and can contribute from day one.
✨Show Off Your Collaboration Skills
Since this role involves working closely with cross-functional teams, be ready to share examples of how you've successfully facilitated discussions and aligned strategies in the past. Highlighting your teamwork will resonate well with the interviewers.
✨Prepare for Health Authority Queries
Familiarise yourself with common Health Authority queries and think about how you would respond. This will demonstrate your proactive approach and understanding of regulatory expectations, which is crucial for the role.
✨Emphasise Your Attention to Detail
In a role where accuracy is key, be prepared to discuss how you ensure high-quality work within tight timelines. Share specific examples of how your planning and prioritisation skills have led to successful outcomes in previous projects.
