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- Tasks: Lead regulatory strategies and collaborate with global teams to improve lives through biotechnology.
- Company: Globally recognised pioneer in Biotechnology focused on high unmet medical needs.
- Benefits: 12-month contract with opportunities for professional growth and impactful work.
- Why this job: Join a mission-driven team making a real difference in healthcare.
- Qualifications: Experience in regulatory affairs and knowledge of drug development processes.
- Other info: Dynamic role with exposure to international regulatory environments.
The predicted salary is between 36000 - 60000 £ per year.
Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of Regulatory Affairs Manager. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to strive for solutions. This is your chance to join them on their global mission to better the lives of those affected by disease and illness.
Responsible for:
- Advising the GRT on regional considerations in developing strategy
- Ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders
- May manage one or more regional leads or support roles
- May participate as a member of: Global Regulatory Team (GRT), Global Development Team (GDT), Clinical Study Team (CST), Label Working Group (LWG), Regional Teams (e.g. IMT, IBT, NAMT)
- Act as a contact with relevant regulatory agencies in fulfilling local obligations by product assignment
- Document and communicate details and outcomes of regulatory agency interactions to GRT and relevant senior management
- Under general supervision participates in core regulatory activities to ensure effective regional agency interactions consistent with the Global Regulatory strategy includes contingency regulatory planning/risk assessment
Knowledge and Skills:
- Regulatory principles
- Working with policies, procedures and SOPs
- Knowledge of relevant legislation and regulations relating to medicinal products
- Awareness of the regulatory procedures in region for MAs, CTAs, post approval changes and amendments, extensions and renewals
- Knowledge of drug development
- Cultural awareness and sensitivity to achieve results across both regional country and international borders
If this role is of interest to you, please apply now!
Regulatory Affairs Manager in London employer: Quanta part of QCS Staffing
Contact Detail:
Quanta part of QCS Staffing Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager in London
✨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 principles and relevant legislation. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your cultural awareness and sensitivity during interviews. We want to see how you can navigate diverse teams and regional considerations, so share examples from your past experiences!
✨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 are proactive about their job search.
We think you need these skills to ace Regulatory Affairs Manager in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Manager role. Highlight your experience with regulatory principles and any relevant legislation you've worked with. We want to see how your skills align with our mission in the life sciences sector!
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 global mission. Don’t forget to mention any specific experiences that relate to the job description.
Showcase Your Teamwork Skills: Since this role involves collaboration with various teams, make sure to highlight your teamwork skills. Share examples of how you've successfully worked with cross-functional teams or managed regional leads in past roles. We love a good team player!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and keep track of it. Plus, it shows you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Quanta part of QCS Staffing
✨Know Your Regulatory Stuff
Make sure you brush up on the latest regulations and guidelines related to medicinal products. Familiarise yourself with the specific legislation in the region you're applying for, as well as any recent changes that might affect the role.
✨Showcase Your Teamwork Skills
Since this role involves collaboration with various teams like the Global Regulatory Team and Clinical Study Team, be ready to share examples of how you've successfully worked in cross-functional teams. Highlight your ability to communicate effectively with different stakeholders.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills and ability to handle regulatory challenges. Think of specific scenarios from your past experience where you had to navigate complex regulatory issues and how you approached them.
✨Cultural Awareness is Key
Given the global nature of the role, demonstrate your understanding of cultural sensitivities and how they impact regulatory affairs. Be prepared to discuss how you've adapted your approach when working with diverse teams or regions.
