At a Glance
- Tasks: Join a dynamic team to learn about Regulatory Affairs in the pharmaceutical industry.
- Company: Leading global healthcare company with a diverse and multicultural environment.
- Benefits: Gain valuable experience through two rotational assignments over two years.
- Other info: Open to applicants eligible to work in the UK; diverse backgrounds welcomed.
- Why this job: Kickstart your career in Regulatory Affairs and make a real impact in drug development.
- Qualifications: MSc, PhD or PharmD in relevant fields; strong interest in Regulatory Affairs.
The predicted salary is between 30000 - 40000 € per year.
The Regulatory Affairs Postgraduate Training Program is an opportunity to discover the global functions of Regulatory Affairs and Regulatory Chemistry, Manufacturing and Controls. Successful candidates will be offered a training position consisting of two rotational assignments, each of 1-year duration, within two different RA functions.
Are you interested to learn more about Regulatory Affairs (RA) and the pharmaceutical industry? After your Master’s, Doctoral or Post-doctoral qualification, do you want a career in Regulatory Affairs? Do you have a collaborative mindset and take ownership of assigned tasks? Are you able to quickly adapt to different teams and concepts, with excellent problem-solving skills? Would you like to work and gain experience in a cross-functional team in the multicultural and diverse environment of a leading global healthcare company?
Responsibilities could include, but are not limited to:
- Interacting with global interdisciplinary project teams to provide strategic regulatory input to development, submission planning, documentation needed, as well as timelines and strategic risks.
- Supporting and/or preparing high quality dossiers, drug substance and/or drug product quality documentation to support global regulatory submissions (e.g. Clinical Trial Applications, Market Authorization Applications, post-approval variations etc.).
- Supporting submission and response activities (planning, preparation, review, coordination, submission).
- Ensuring regulatory compliance by creating awareness of requirements and guidelines, facilitating timely submission of variations and participation in the change control process.
- Supporting the development and maintenance of globally consistent product information.
- Supporting the Regulatory Intelligence group analysing the EU Regulatory Framework and informing the internal RA community.
- Monitoring, searching for and evaluating legislation, as well as guidelines from different sources.
Duration and start of training: 2 years with an expected start date beginning January 2027.
Deadline for applications: June 3, 2026.
Interviews: September 2026.
Minimum requirements:
- Strong interest in Regulatory Affairs and Drug Development.
- Completion of an MSc, PhD or PharmD in Pharmaceutical Sciences/Pharmacy/Life Sciences or equivalent within the last 24 months.
- Fluency in English (written and spoken); CV and Cover letter in English required to apply.
- For your cover letter, please consider addressing the following: Articulate clearly your desire to join this particular program, your specific motivations for Regulatory Affairs and how this opportunity will facilitate your future career ambitions in Regulatory Affairs.
- Ready to expand your knowledge and are open minded with an international outlook.
- Strong interpersonal skills i.e. can demonstrate your ability to communicate well with people from a variety of backgrounds/cultures and at different hierarchical levels inside and outside the company.
Please note that we can only accept applicants who are eligible to work in the UK. Novartis is an equal opportunity employer committed to embracing and leveraging diverse backgrounds.
Skills Desired: Clinical Study Reports, Data Analysis, Documentation Management, Lifesciences, Operational Excellence, Regulatory Compliance.
Regulatory Affairs Postgraduate Program UK in London employer: Novartis
At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic and inclusive work culture that fosters collaboration and innovation. Our Regulatory Affairs Postgraduate Training Program provides unique opportunities for professional growth through hands-on experience in a global healthcare environment, ensuring that you are well-prepared for a rewarding career in Regulatory Affairs. With a commitment to diversity and equal opportunity, we empower our employees to thrive and make a meaningful impact in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Affairs Postgraduate Program UK in London
✨Tip Number 1
Network like a pro! Reach out to professionals in Regulatory Affairs on LinkedIn or at industry events. A friendly chat can open doors and give you insights that job descriptions just can't.
✨Tip Number 2
Prepare for interviews by researching the company and its recent projects. Show us that you're not just interested in any job, but specifically in how you can contribute to our Regulatory Affairs team.
✨Tip Number 3
Practice your problem-solving skills with real-world scenarios. We love candidates who can think on their feet, so be ready to tackle some hypothetical challenges during your interview.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows us you’re serious about joining our team.
We think you need these skills to ace Regulatory Affairs Postgraduate Program UK in London
Some tips for your application 🫡
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Make sure to clearly express why you're excited about the Regulatory Affairs Postgraduate Program and how it aligns with your career goals. We want to see your passion for RA and how you can contribute to our team.
Tailor Your CV:Don’t just send out the same CV for every application. Tailor it to highlight your relevant experiences and skills that match the job description. We’re looking for candidates who can demonstrate their strong interest in Regulatory Affairs and Drug Development.
Showcase Your Interpersonal Skills:In your application, don’t forget to mention your ability to communicate effectively with diverse teams. We value collaboration, so share examples of how you've worked well with others from different backgrounds or cultures.
Apply Through Our Website:Make sure to apply through our official website to ensure your application gets the attention it deserves. We’re excited to see what you bring to the table, so don’t miss out on this opportunity!
How to prepare for a job interview at Novartis
✨Know Your Regulatory Affairs
Make sure you brush up on the basics of Regulatory Affairs and the pharmaceutical industry. Understand key concepts like drug development, submission processes, and compliance requirements. This knowledge will help you answer questions confidently and show your genuine interest in the field.
✨Tailor Your Cover Letter
When writing your cover letter, be specific about why you want to join this programme. Highlight your motivations for pursuing a career in Regulatory Affairs and how this opportunity aligns with your future ambitions. A personalised cover letter can set you apart from other candidates.
✨Showcase Your Interpersonal Skills
Since the role involves working in cross-functional teams, be prepared to discuss your interpersonal skills. Share examples of how you've effectively communicated with diverse groups or resolved conflicts. This will demonstrate your ability to adapt and collaborate in a multicultural environment.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities. Think of examples from your academic or professional experience where you faced challenges and how you overcame them. This will showcase your critical thinking skills and readiness for the dynamic nature of Regulatory Affairs.
