At a Glance
- Tasks: Lead regulatory strategies for innovative pharmaceutical products across EMEA.
- Company: Global pharmaceutical leader focused on eye health and patient outcomes.
- Benefits: Competitive salary, comprehensive benefits, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to innovation and patient-centric solutions.
- Why this job: Make a real impact in healthcare by shaping regulatory pathways for life-changing therapies.
- Qualifications: 8+ years in regulatory affairs with strong EU/UK knowledge and collaboration skills.
The predicted salary is between 70000 - 90000 € per year.
The Company is a global, science-led pharmaceutical organization with a long-established heritage and a focused commitment to eye health. The company operates across multiple global regions and is dedicated to developing innovative ophthalmic therapies that improve patient outcomes. Its mission is to deliver meaningful value to patients and healthcare systems through scientific expertise and a patient-centric approach.
We are seeking an experienced EMEA Regional Regulatory Lead to define and execute regulatory strategies supporting the development and registration of pharmaceutical pipeline products across Europe, the Middle East, and Africa.
You will act as a key regional regulatory expert, partnering with global, regional, and local stakeholders to ensure regulatory compliance, anticipate evolving regulatory landscapes, and enable successful development and approvals across the EMEA region. You will also support affiliate-level regulatory activities for selected countries within the region.
- Lead EMEA regulatory strategy development for pipeline development programmes, aligned with global regulatory plans
- Represent the EMEA region in global regulatory teams, providing strategic and regional input
- Own regional regulatory strategy across the product lifecycle
- Oversee selected affiliate regulatory activities, including authority interactions and country-specific submission strategies
- Build and maintain relationships with regulatory authorities across EMEA
- Conduct regulatory intelligence and competitor/landscape monitoring to support risk and opportunity planning
- Monitor changes in regulatory frameworks and assess impact on development and lifecycle strategies
- Review promotional and packaging materials for regulatory compliance
- Support regulatory SOPs, lifecycle management, and cross-functional regulatory deliverables
Requirements:
- 8+ years of experience in medicinal regulatory affairs in Europe/UK
- Proven experience in regulatory strategy, submissions, and lifecycle management
- Experience in Marketing Authorization Applications and clinical development support
- Strong understanding of EU/UK regulatory frameworks and legislation
- Strong stakeholder management and cross-functional collaboration skills
- Excellent written and verbal English
Associate Director Regulatory Compliance in London employer: Barrington James
As a global leader in the pharmaceutical industry, our company offers an exceptional work environment that prioritises innovation and patient-centric solutions. Employees benefit from a collaborative culture that fosters professional growth through continuous learning opportunities and engagement with diverse teams across the EMEA region. With a strong commitment to eye health and a focus on regulatory excellence, we provide a unique platform for individuals to make a meaningful impact in healthcare while enjoying a supportive and dynamic workplace.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director Regulatory Compliance in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory compliance field on LinkedIn or at industry events. Building connections can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of EU/UK regulatory frameworks. Be ready to discuss how your experience aligns with the company's mission and how you can contribute to their innovative ophthalmic therapies.
✨Tip Number 3
Showcase your stakeholder management skills during interviews. Share specific examples of how you've successfully collaborated with cross-functional teams and navigated complex regulatory landscapes in your previous roles.
✨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 with our company.
We think you need these skills to ace Associate Director Regulatory Compliance in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Associate Director Regulatory Compliance role. Highlight your experience in regulatory affairs, especially in the EMEA region, and showcase any relevant achievements that align with the job description.
Craft a Compelling Cover Letter:Your cover letter should tell us why you're the perfect fit for this role. Use it to explain how your background in regulatory strategy and compliance can contribute to our mission of improving patient outcomes through innovative therapies.
Showcase Your Stakeholder Management Skills:Since this role involves a lot of collaboration, make sure to highlight your experience in managing relationships with regulatory authorities and cross-functional teams. We want to see how you’ve successfully navigated complex regulatory landscapes in the past.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team at StudySmarter!
How to prepare for a job interview at Barrington James
✨Know Your Regulatory Stuff
Make sure you brush up on the latest EU/UK regulatory frameworks and legislation. Be ready to discuss how your experience aligns with the company's focus on innovative ophthalmic therapies and how you can contribute to their mission.
✨Showcase Your Stakeholder Skills
Prepare examples of how you've successfully managed relationships with regulatory authorities and cross-functional teams. Highlight specific instances where your collaboration led to successful outcomes in regulatory submissions or strategy development.
✨Anticipate Questions on Strategy
Expect questions about how you would approach developing regulatory strategies for pipeline products. Think through potential challenges in the EMEA region and be ready to share your insights on navigating these complexities.
✨Communicate Clearly and Confidently
Since excellent written and verbal English is a must, practice articulating your thoughts clearly. Use concise language when discussing your past experiences and ensure you convey your passion for regulatory compliance and patient-centric approaches.
