At a Glance
- Tasks: Lead a dynamic team in Regulatory Affairs and shape strategies for innovative medicines.
- Company: Join a global biopharmaceutical leader focused on breakthrough therapies.
- Benefits: Enjoy hybrid working, competitive salary, and a supportive environment.
- Other info: Collaborative culture with excellent career growth opportunities across Europe.
- Why this job: Make a real impact on healthcare by influencing key regulatory outcomes.
- Qualifications: Experience in Regulatory Affairs and strong leadership skills required.
The predicted salary is between 70000 - 90000 £ per year.
Apsida Life Science are currently partnering with a global biopharmaceutical company recognised for developing innovative medicines that address complex and serious diseases. The organisation combines strong scientific expertise with a patient-first approach, focusing on improving standards of care through breakthrough therapies and close collaboration with healthcare systems.
Location: M4 Corridor
Responsibilities:
- Lead and manage a team of Regulatory Affairs professionals, providing guidance and strategic direction.
- Act as the primary interface with European Health Authorities, including EMA.
- Define and implement regulatory strategies across a portfolio spanning early development, late-stage, and marketed products.
- Provide leadership and regulatory support to affiliate teams across the European region.
- Drive delivery of regulatory submissions and ensure alignment with global and regional objectives.
- Collaborate cross-functionally to support product development, approvals, and lifecycle management.
Qualifications:
- Significant experience in Regulatory Affairs within the pharmaceutical or biotechnology industry.
- Proven leadership experience managing and developing regulatory teams.
- Strong knowledge of European regulatory frameworks and Health Authority interactions (EMA).
- Experience across multiple stages of the product lifecycle (development to post-marketing).
- Excellent stakeholder management and cross-functional collaboration skills.
- Strong strategic mindset with the ability to drive regulatory outcomes in a complex environment.
Position Highlights:
- Leadership role managing and developing a high-performing Regulatory Affairs team across Europe.
- Strategic ownership of a diverse product portfolio spanning early development through to marketed assets.
- Direct interaction with EMA and European Health Authorities, influencing key regulatory outcomes.
- Opportunity to work within a globally recognised biopharma with strong R&D investment and pipeline.
- High visibility role with cross-functional collaboration across global and regional teams.
- Hybrid working model within a supportive, collaborative, and innovation-driven environment.
If you are interested in learning more, please contact Geneva Jones at Apsida Life Science: Geneva.Jones@apsida.com
Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry.
Associate Director Regulatory Affairs in London employer: Apsida Life Science
Apsida Life Science is an exceptional employer, offering a dynamic and innovative work environment within the thriving M4 Corridor. Employees benefit from a hybrid working model that promotes collaboration and creativity, alongside opportunities for professional growth in a globally recognised biopharmaceutical company. With a strong focus on leadership development and strategic influence in regulatory affairs, this role provides a unique chance to make a meaningful impact on healthcare outcomes across Europe.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director Regulatory Affairs in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the Regulatory Affairs field, especially those who work with European Health Authorities. Attend industry events or webinars to make connections and learn about potential job openings.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of European regulatory frameworks and recent developments in the biopharmaceutical industry. We want you to be able to discuss how your experience aligns with the role and the company's mission.
✨Tip Number 3
Showcase your leadership skills! Be ready to share examples of how you've successfully managed teams and driven regulatory outcomes. Highlight your strategic mindset and ability to collaborate cross-functionally.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re here to support you throughout the process, so don’t hesitate to reach out if you have questions.
We think you need these skills to ace Associate Director Regulatory Affairs in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Associate Director, Regulatory Affairs role. Highlight your experience in managing regulatory teams and your knowledge of European regulatory frameworks. 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 and how you can contribute to our mission at Apsida Life Science. Keep it concise but impactful – we love a good story!
Showcase Your Leadership Skills:Since this role involves leading a team, make sure to showcase your leadership experience. Share examples of how you've successfully managed teams and driven regulatory outcomes. We’re looking for someone who can inspire and guide others!
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss any important updates. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Apsida Life Science
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of European regulatory frameworks and the EMA. Be ready to discuss how your experience aligns with the responsibilities of the role, especially in leading regulatory submissions and interacting with health authorities.
✨Showcase Your Leadership Skills
Since this role involves managing a team, be prepared to share examples of how you've successfully led and developed regulatory teams in the past. Highlight your strategic mindset and how you've driven outcomes in complex environments.
✨Prepare for Cross-Functional Collaboration
This position requires collaboration across various teams. Think of specific instances where you've worked cross-functionally to support product development or approvals. Be ready to explain how you navigated challenges and achieved alignment.
✨Ask Insightful Questions
At the end of the interview, don’t forget to ask questions that show your interest in the company and the role. Inquire about their current projects, the team dynamics, or how they measure success in regulatory affairs. This shows you're genuinely interested and engaged.
