Director Europe Regulatory Policy
Director Europe Regulatory Policy

Director Europe Regulatory Policy

Full-Time 43200 - 72000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead regulatory policy work to shape the environment for our medicines across Europe.
  • Company: Join GSK, a global biopharma company with bold ambitions for patient health.
  • Benefits: Hybrid working model, professional growth opportunities, and a commitment to inclusivity.
  • Why this job: Make a meaningful impact on patient health while collaborating with top professionals.
  • Qualifications: Bachelor's in life sciences or related field; experience in regulatory affairs required.
  • Other info: Dynamic role with strong visibility and the chance to influence healthcare policy.

The predicted salary is between 43200 - 72000 £ per year.

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success.

The Director of Europe Regulatory Policy leads regulatory policy work that shapes the external environment for our medicines. You will work across teams in Europe and globally to develop policy priorities, deliver advocacy, and translate complex regulatory change into practical internal guidance. We value clear thinking, collaborative leadership, and the ability to build trusted relationships with regulators and partners. This role offers strong visibility, professional growth, and the chance to make a meaningful impact for patients and GSK.

Responsibilities
  • Develop and maintain Europe/EU regulatory policy, advocacy, and intelligence priorities to support and advance GSK's portfolio.
  • Provide expert interpretation and advice on new legislation, guidelines, and regulatory policies, assessing their impact on GSK and our portfolio.
  • Build and maintain strong relationships with external stakeholders, including regulatory agencies, industry trade associations, and multi-stakeholder initiatives, to develop external insights and to advance GSK’s policy objectives and positions.
  • Collaborate with internal teams to develop and execute regulatory policy and advocacy strategies in the Europe/EU region.
  • Lead asset-specific global regulatory policy and advocacy strategy for select priority assets.
  • Lead global regulatory policy and advocacy strategy for select enterprise-level policy priorities.
  • May brief and provide support to senior leaders on external developments and engagements.
Basic Qualification
  • Bachelor's Degree in life sciences, pharmacy, law, public policy, or a related field.
  • Experience in regulatory affairs with expertise across all phases of the medicines development process.
  • Proven track record in medicines regulatory policy and advocacy and a broad understanding of the European/EU regulatory environment.
  • Experience analysing complex regulatory information and communicating analyses clearly and succinctly.
Preferred Qualification
  • Advanced degree (MSc, PhD, Law/JD, PharmD) or postgraduate qualification relevant to Regulatory Affairs.
  • In-depth knowledge of medicines development laws, regulations, and practices affecting the pharmaceutical industry in Europe/EU and familiarity with regulatory submission processes.
  • Direct experience interacting with European regulatory agencies and health authorities (EMA and national competent authorities).
  • Skilled at working in matrix environments and delivering impactful results.
  • Strong interpersonal, communication (oral/written English), influencing, and negotiation skills and the ability to build effective internal and external networks.
Working Pattern

This role is based in the United Kingdom or Belgium and operates on a hybrid working model. You will be expected to spend regular time onsite to collaborate with colleagues and partners. Occasional travel across Europe may be required.

How to apply

If this role inspires you and you meet the basic qualifications, we encourage you to apply. Please submit your CV and a short cover letter outlining your relevant experience and what motivates you to join GSK in this role. We welcome applicants from diverse backgrounds and experiences and are committed to creating an inclusive workplace where all can thrive.

Equal Opportunity Employer

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Accommodations

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities, contact UKRecruitment.Adjustments@gsk.com where you can also request a call.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.

Director Europe Regulatory Policy employer: GlaxoSmithKline

GSK is an exceptional employer, offering a dynamic work environment in the heart of London or Belgium, where innovation meets collaboration. With a strong commitment to employee growth and a culture that prioritises patient impact, GSK provides unique opportunities for professional development and meaningful contributions to global health. The hybrid working model fosters flexibility, while the company's dedication to inclusivity ensures that all employees can thrive and make a difference.
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Contact Detail:

GlaxoSmithKline Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Director Europe Regulatory Policy

✨Tip Number 1

Network like a pro! Reach out to people in your industry on LinkedIn or at events. A friendly chat can lead to opportunities you might not find on job boards.

✨Tip Number 2

Prepare for interviews by researching GSK's recent projects and regulatory changes. Show them you’re not just interested in the role, but also in their mission to impact health positively.

✨Tip Number 3

Practice your pitch! Be ready to explain how your experience aligns with GSK’s goals. Keep it concise and focus on how you can contribute to their ambitious plans.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the GSK team.

We think you need these skills to ace Director Europe Regulatory Policy

Regulatory Affairs Expertise
Policy Development
Advocacy Skills
Stakeholder Engagement
Analytical Skills
Communication Skills
Interpersonal Skills
Negotiation Skills
Knowledge of European Regulatory Environment
Experience with Regulatory Submission Processes
Collaboration in Matrix Environments
Understanding of Medicines Development Laws
Ability to Translate Complex Information
Project Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the role of Director Europe Regulatory Policy. Highlight your relevant experience in regulatory affairs and any specific achievements that align with GSK's goals. We want to see how your background fits into our ambitious plans!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills can help us impact the health of 2.5 billion people. Keep it concise but engaging – we love a good story!

Showcase Your Communication Skills: Since this role involves building relationships and influencing stakeholders, make sure your written application reflects your strong communication skills. Clear, succinct language will show us you can translate complex regulatory information effectively.

Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way to ensure your application gets the attention it deserves. Plus, it shows you’re keen on joining our team at GSK!

How to prepare for a job interview at GlaxoSmithKline

✨Know Your Regulatory Stuff

Make sure you brush up on the latest European regulatory policies and guidelines. GSK is looking for someone who can interpret complex regulations, so be prepared to discuss how recent changes might impact their portfolio.

✨Build Relationships

Since this role involves collaborating with various stakeholders, think about how you can demonstrate your relationship-building skills. Have examples ready of how you've successfully worked with regulators or industry partners in the past.

✨Showcase Your Advocacy Skills

Be ready to talk about your experience in advocacy and how you've influenced policy decisions. GSK values clear thinking and impactful communication, so highlight any successful strategies you've implemented in previous roles.

✨Prepare for Scenario Questions

Expect scenario-based questions that assess your problem-solving abilities in regulatory contexts. Think through potential challenges you might face in this role and how you would approach them, showcasing your analytical skills and strategic thinking.

Director Europe Regulatory Policy
GlaxoSmithKline
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