Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead regulatory activities and ensure compliance across diverse pharmaceutical products.
- Company: Join a dynamic pharmaceutical company focused on innovation and compliance.
- Benefits: Competitive salary, professional development, and opportunities for mentorship.
- Why this job: Make a real impact in the pharmaceutical industry while leading a dedicated team.
- Qualifications: Degree in Life Sciences and experience in Regulatory Affairs required.
- Other info: Opportunity for career growth and to shape regulatory processes.
The predicted salary is between 36000 - 60000 £ per year.
We are hiring a Regulatory Affairs Manager to support regulatory activities across a diverse pharmaceutical portfolio, including both marketed and pre-approval supply pathways. This role suits experienced regulatory professionals or individuals ready to step up into broader responsibility. The RA Manager will be managing 2 direct reports.
Key responsibilities
- Lead regulatory activities across assigned products and regions, ensuring compliance with applicable legislation and Good Regulatory Practice.
- Provide regulatory guidance to cross‑functional teams, including support for special access, pre‑approval, or non‑standard supply scenarios where required.
- Support regulatory capability and process development, contributing to continuous improvement and mentoring within the regulatory function.
About you
- Degree in Life Sciences or a related discipline.
- Experience in Regulatory Affairs within the pharmaceutical industry.
- Strong understanding of regulatory frameworks, preferably in multiple regions.
- Comfortable working independently and collaboratively.
- Previous people management experience is welcome but not essential.
Regulatory Affairs Manager in England employer: GxPeople Global
Contact Detail:
GxPeople Global Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager in England
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory frameworks. We recommend creating a cheat sheet of key regulations and recent changes in the industry to impress your interviewers.
✨Tip Number 3
Showcase your leadership skills! If you’ve managed teams before, be ready to discuss your approach to mentoring and developing others. We want to see how you can contribute to our regulatory capability and process development.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Regulatory Affairs Manager in England
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Regulatory Affairs, especially any relevant roles in the pharmaceutical industry. We want to see how your background aligns with the key responsibilities of the Regulatory Affairs Manager position.
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. Don’t forget to mention any experience you have with compliance and regulatory frameworks.
Showcase Your Leadership Skills: If you've got people management experience, make sure to highlight it! Even if you haven't managed a team before, share examples of how you've led projects or mentored others. We value collaboration and guidance in our team.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. We can’t wait to see what you bring to the table!
How to prepare for a job interview at GxPeople Global
✨Know Your Regulatory Stuff
Make sure you brush up on the latest regulatory frameworks relevant to the pharmaceutical industry. Be ready to discuss specific regulations and how they apply to both marketed and pre-approval products. This shows you’re not just familiar with the basics but are also up-to-date with current practices.
✨Showcase Your Leadership Skills
Since this role involves managing direct reports, be prepared to share examples of your leadership experience. Talk about how you've mentored others or led projects in the past. Even if you haven't managed a team before, think of situations where you've taken the lead or influenced a group.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific regulatory challenges, especially in special access or non-standard supply scenarios. Think through potential scenarios beforehand and outline your thought process. This will demonstrate your problem-solving skills and ability to provide regulatory guidance.
✨Emphasise Continuous Improvement
The job mentions contributing to process development and continuous improvement. Be ready to discuss any initiatives you've been part of that aimed at improving regulatory processes. Highlight your proactive approach and willingness to mentor others in the regulatory function.
