EMEA Regulatory Lead & UKI Cluster Director
EMEA Regulatory Lead & UKI Cluster Director

EMEA Regulatory Lead & UKI Cluster Director

Full-Time 48000 - 72000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory strategies across Europe, the Middle East, and Africa for a global pharmaceutical company.
  • Company: Join a leading global pharmaceutical company with an inclusive work culture.
  • Benefits: Full-time role with competitive salary and opportunities for professional growth.
  • Why this job: Make a significant impact on healthcare by driving regulatory affairs in a dynamic environment.
  • Qualifications: 8+ years in regulatory affairs with strong communication and collaboration skills.
  • Other info: No remote work; thrive in a supportive and diverse workplace.

The predicted salary is between 48000 - 72000 Β£ per year.

A global pharmaceutical company is seeking an experienced EMEA Regional Regulatory Lead to drive regulatory strategies across Europe, the Middle East, and Africa. In this role, you will manage all regulatory affairs activities for the UK & Ireland and lead multi-regional product strategies.

Qualified candidates must have a minimum of 8 years of experience in regulatory affairs, particularly with MHRA and HPRA, and possess strong communication and collaboration skills. This full-time role requires no remote work and offers an inclusive work environment.

EMEA Regulatory Lead & UKI Cluster Director employer: Santen

Join a leading global pharmaceutical company that prioritises employee development and fosters a collaborative work culture. With a strong commitment to inclusivity, you will have access to comprehensive benefits and opportunities for professional growth, all while working in a dynamic environment that values your contributions to regulatory strategies across Europe, the Middle East, and Africa.
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Contact Detail:

Santen Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land EMEA Regulatory Lead & UKI Cluster Director

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who have experience with regulatory affairs. A friendly chat can lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of MHRA and HPRA regulations. We all know that confidence is key, so practice answering common interview questions related to regulatory strategies in a collaborative environment.

✨Tip Number 3

Showcase your communication skills! During interviews, be sure to highlight examples of how you've successfully collaborated with cross-functional teams. This will demonstrate your ability to lead multi-regional product strategies effectively.

✨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 and engaged in their job search.

We think you need these skills to ace EMEA Regulatory Lead & UKI Cluster Director

Regulatory Affairs
MHRA Knowledge
HPRA Knowledge
Communication Skills
Collaboration Skills
Regulatory Strategy Development
Multi-Regional Product Management
Experience in Pharmaceutical Industry
Project Management
Stakeholder Engagement
Problem-Solving Skills
Attention to Detail
Adaptability

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs, especially with MHRA and HPRA. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects and achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the EMEA Regulatory Lead position. We love seeing your personality come through, so feel free to share your passion for regulatory strategies.

Showcase Your Communication Skills: Since strong communication is key for this role, make sure your application reflects that. We recommend using clear, concise language and structuring your thoughts logically. This will demonstrate your ability to communicate effectively right from the start!

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and you’ll be all set!

How to prepare for a job interview at Santen

✨Know Your Regulations

Make sure you brush up on the latest regulations from MHRA and HPRA. Being able to discuss specific regulatory frameworks and how they impact product strategies will show that you're not just familiar with the basics, but that you’re ready to lead.

✨Showcase Your Experience

With a minimum of 8 years in regulatory affairs, you’ll want to highlight your relevant experiences. Prepare examples of past projects where you successfully navigated complex regulatory landscapes, especially in the EMEA region.

✨Communication is Key

Since this role requires strong communication skills, practice articulating your thoughts clearly and confidently. Think about how you can convey complex regulatory information in a way that’s easy to understand for different stakeholders.

✨Collaborative Mindset

This position involves leading multi-regional product strategies, so be ready to discuss how you’ve worked collaboratively in the past. Share examples of how you’ve built relationships across teams and regions to achieve regulatory success.

EMEA Regulatory Lead & UKI Cluster Director
Santen
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  • EMEA Regulatory Lead & UKI Cluster Director

    Full-Time
    48000 - 72000 Β£ / year (est.)
  • S

    Santen

    100-200
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