At a Glance
- Tasks: Engage in a two-year training programme with rotations in Regulatory Affairs functions.
- Company: Join a leading global healthcare company committed to innovation.
- Benefits: Gain invaluable experience, mentorship, and exposure to global regulatory processes.
- Other info: Open to diverse backgrounds; start date in January 2027.
- Why this job: Kickstart your career in Regulatory Affairs and make a real impact in drug development.
- Qualifications: Recent MSc, PhD or PharmD graduates with a passion for Regulatory Affairs.
The predicted salary is between 30000 - 40000 £ per year.
Position Overview
The Regulatory Affairs Postgraduate Training Program offers a two-year training experience comprising two one-year rotational assignments in distinct RA functions. Participants will gain exposure to global Regulatory Affairs, Regulatory Chemistry, Manufacturing and Controls across a leading global healthcare company.
Responsibilities
- Interact with global interdisciplinary project teams to provide strategic regulatory input for development, submission planning, documentation and timelines.
- Support and/or prepare high-quality dossiers and drug substance/drug product quality documentation for global regulatory submissions (e.g., Clinical Trial Applications, Market Authorization Applications, post-approval variations).
- Adapt dossiers to meet specific requirements in various countries and regions.
- Plan, prepare, review, coordinate and submit regulatory submissions and responses.
- Ensure regulatory compliance by creating awareness of requirements and guidelines, facilitating timely submission of variations, and participating in the change control process.
- Develop and maintain globally consistent product information.
- Support the Regulatory Intelligence group in analysing the EU regulatory framework and informing the internal RA community.
- Monitor, search for and evaluate legislation and guidelines from different sources.
Qualifications
- Strong interest in Regulatory Affairs and drug development.
- Completion of an MSc, PhD or PharmD in Pharmaceutical Sciences, Pharmacy, Life Sciences or an equivalent within the last 24 months.
- Fluency in English (written and spoken).
- Open-minded with an international outlook and ready to expand knowledge.
- Strong interpersonal skills; ability to communicate effectively across cultures and hierarchies.
Program Details
- Duration: 2 years, with expected start date January 2027.
Legal Notice
Novartis is an equal-opportunity employer committed to embracing and leveraging diverse backgrounds. Applicants must be eligible to work in the United Kingdom.
Regulatory Affairs Postgraduate Program UK employer: Job Search Place Limited
Join a leading global healthcare company that prioritises employee development and fosters a collaborative work culture. The Regulatory Affairs Postgraduate Program offers unique opportunities for growth through hands-on experience in diverse regulatory functions, while being part of a team that values innovation and compliance. With a commitment to diversity and inclusion, this programme not only equips you with essential skills but also allows you to contribute to meaningful projects that impact global health.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Affairs Postgraduate Program UK
✨Tip Number 1
Network like a pro! Reach out to professionals in Regulatory Affairs on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream role.
✨Tip Number 2
Prepare for interviews by researching the company and its regulatory processes. We recommend practising common interview questions and having your own questions ready to show your interest in their work.
✨Tip Number 3
Showcase your skills! Bring examples of your past projects or experiences that relate to regulatory submissions. We want to see how you can contribute to the team right from the start.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take the initiative to engage directly with us.
We think you need these skills to ace Regulatory Affairs Postgraduate Program UK
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects your interest in Regulatory Affairs and highlights any relevant experience or education. We want to see how your background aligns with the role, so don’t be shy about showcasing your MSc, PhD, or PharmD!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about Regulatory Affairs and how you can contribute to our team. Keep it engaging and make sure to mention your international outlook and strong interpersonal skills.
Showcase Your Skills:In your application, highlight your ability to communicate effectively across cultures and hierarchies. We value strong interpersonal skills, so give us examples of how you've successfully collaborated in diverse teams or projects.
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of being noticed. It’s straightforward and ensures your application gets to the right people. Plus, we love seeing candidates who take the initiative!
How to prepare for a job interview at Job Search Place Limited
✨Know Your Regulatory Affairs
Make sure you brush up on the latest trends and regulations in the field of Regulatory Affairs. Familiarise yourself with key terms and concepts related to drug development, as well as the specific requirements for submissions in different countries. This will show your genuine interest and understanding of the role.
✨Prepare Your Examples
Think of specific examples from your academic or professional experience that demonstrate your skills in communication, teamwork, and problem-solving. Be ready to discuss how you've worked in interdisciplinary teams or tackled challenges in regulatory compliance. This will help you stand out as a candidate who can contribute effectively.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s approach to Regulatory Affairs and the training programme itself. This not only shows your enthusiasm but also helps you gauge if the company aligns with your career goals. Questions about their global strategies or recent regulatory changes can spark engaging conversations.
✨Show Your International Mindset
Since the role requires an international outlook, be prepared to discuss any experiences you have had working or studying abroad. Highlight your ability to adapt to different cultures and communicate effectively across hierarchies. This will demonstrate that you are ready to thrive in a global environment.
