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

EU Regulatory Affairs Lead - Medicines & Devices

Full-Time 60000 - 80000 £ / 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 real difference in public health by shaping policies for medicines and medical devices.
  • Qualifications: Experience in public sector engagements and knowledge of health and life sciences.
  • Other info: Full-time, permanent role with at least 8 on-site days per month.

The predicted salary is between 60000 - 80000 £ 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 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

✨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 a lead on your dream job!

✨Tip Number 2

Prepare for interviews by brushing up on current EU regulatory policies and trends in medicines and devices. We recommend creating a cheat sheet of key topics to discuss, so you can impress your interviewers with your knowledge and passion for the field.

✨Tip Number 3

Showcase your stakeholder engagement skills! Think of examples from your past experiences where you successfully managed relationships or led projects. We want to hear about how you navigated challenges and achieved results—this is your chance to shine!

✨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 engage directly with us—so go ahead and submit that application!

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

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 how you can contribute to our team.

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 related to 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 genuinely 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’ve navigated complex discussions. 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 specific 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 or reports you’ve drafted in the past. Discuss your approach to writing these documents and how you ensure they meet the needs of government leaders. This will showcase your analytical skills and attention to detail.

EU Regulatory Affairs Lead - Medicines & Devices
Mhra

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