EU Regulatory Affairs Lead - Medicines & Devices in London
EU Regulatory Affairs Lead - Medicines & Devices

EU Regulatory Affairs Lead - Medicines & Devices in London

London Full-Time 60000 - 75000 £ / year (est.) Home office (partial)
Mhra

At a Glance

  • Tasks: Lead EU regulatory initiatives and engage with stakeholders in health and life sciences.
  • Company: Public health regulatory agency in Greater London with a focus on medicines and devices.
  • Benefits: Hybrid work environment, competitive salary, and opportunities for professional growth.
  • Why this job: Make a significant impact on public health through policy recommendations and cross-project coordination.
  • Qualifications: Experience in public sector engagements and knowledge of health and life sciences.

The predicted salary is between 60000 - 75000 £ per year.

A public health regulatory agency in Greater London seeks a Principal Policy Lead to oversee EU regulatory initiatives in medicines and medical devices. The successful candidate will manage stakeholder engagement, coordinate cross-MHRA projects, and draft policy recommendations for government leaders.

This full-time, permanent role offers a hybrid work environment requiring at least 8 on-site days per month. An ideal candidate will have experience in public sector engagements and understanding of health and life sciences.

EU Regulatory Affairs Lead - Medicines & Devices in London employer: Mhra

As a leading public health regulatory agency in Greater London, we pride ourselves on fostering a collaborative and inclusive work culture that empowers our employees to make a meaningful impact in the health and life sciences sector. With a strong focus on professional development, we offer numerous growth opportunities and a supportive environment that values innovation and stakeholder engagement. Our hybrid work model ensures flexibility while maintaining a strong team dynamic, making us an excellent employer for those looking to contribute to vital regulatory initiatives.
Mhra

Contact Detail:

Mhra Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land EU Regulatory Affairs Lead - Medicines & Devices in London

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs space, especially those who have experience with EU regulations. Use platforms like LinkedIn to connect and engage with them; you never know who might have insider info on job openings.

✨Tip Number 2

Prepare for interviews by brushing up on current EU regulatory trends in medicines and devices. We recommend creating a list of potential questions and practising your responses. This will help you feel more confident and ready to impress!

✨Tip Number 3

Showcase your stakeholder engagement skills! During interviews, share specific examples of how you've successfully managed relationships in previous roles. This is crucial for the Principal Policy Lead position, so make sure to highlight your experience.

✨Tip Number 4

Don’t forget to apply through our website! We’ve got loads of resources to help you land that dream job. Plus, applying directly can sometimes give you an edge over other candidates. So, get your application in and let’s make it happen!

We think you need these skills to ace EU Regulatory Affairs Lead - Medicines & Devices in London

Stakeholder Engagement
Policy Development
Project Coordination
Public Sector Experience
Knowledge of Health and Life Sciences
Regulatory Compliance
Communication Skills
Analytical Skills
Cross-Functional Collaboration
Drafting Policy Recommendations
Strategic Thinking
Problem-Solving Skills
Adaptability
Team Leadership

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the role of EU Regulatory Affairs Lead. Highlight your experience in public sector engagements and any relevant projects you've managed. We want to see how your background aligns with our needs!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about regulatory affairs in medicines and devices. Share specific examples of your work that demonstrate your expertise and enthusiasm for the role.

Showcase Stakeholder Engagement Skills: Since this role involves managing stakeholder engagement, be sure to highlight any relevant experiences. We love to see how you've successfully coordinated with different parties and navigated complex projects in the past.

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves. Plus, it’s super easy!

How to prepare for a job interview at Mhra

✨Know Your Regulations

Make sure you brush up on the latest EU regulations regarding medicines and medical devices. Being able to discuss specific policies and their implications will show that you're not just familiar with the field, but that you're also passionate about it.

✨Engage Stakeholders Effectively

Prepare examples of how you've successfully engaged with stakeholders in the past. Think about your communication strategies and how you navigated different interests. This will demonstrate your ability to manage relationships, which is crucial for this role.

✨Cross-Project Coordination Skills

Be ready to talk about your experience coordinating projects across different teams or departments. Highlight any tools or methods you used to ensure smooth collaboration, as this will be key in managing cross-MHRA projects.

✨Drafting Policy Recommendations

Bring along samples of policy recommendations you've drafted, if possible. Discuss your approach to writing these documents and how you ensure they are clear and actionable. This will showcase your expertise and readiness for the responsibilities of the role.

EU Regulatory Affairs Lead - Medicines & Devices in London
Mhra
Location: London

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