European Regulatory Affairs Lead - Strategy & Lifecycle in Maidenhead
European Regulatory Affairs Lead - Strategy & Lifecycle

European Regulatory Affairs Lead - Strategy & Lifecycle in Maidenhead

Maidenhead Full-Time 36000 - 60000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead the strategy for regulatory approvals of innovative pharmaceutical products.
  • Company: Global biopharmaceutical company based in the UK with a strong reputation.
  • Benefits: Competitive salary, travel opportunities, and a chance to shape healthcare.
  • Why this job: Make a real difference in patient lives through impactful regulatory strategies.
  • Qualifications: Experience in European Regulatory strategy and a background in life sciences.
  • Other info: Dynamic role with opportunities for professional growth and development.

The predicted salary is between 36000 - 60000 £ per year.

A global biopharmaceutical company in the UK is seeking a Regulatory Affairs professional. You will implement registration strategies for regulatory approvals of pharmaceutical products. This role requires a sound knowledge of pharmaceutical regulations, strong organizational capabilities, and the ability to effectively prioritize multiple projects. The ideal candidate has experience in European Regulatory strategy development and a life sciences education. Expect travel of approximately 10%.

European Regulatory Affairs Lead - Strategy & Lifecycle in Maidenhead employer: AbbVie Inc

Join a leading global biopharmaceutical company in the UK, where you will be part of a dynamic team dedicated to advancing healthcare through innovative regulatory strategies. Our collaborative work culture fosters professional growth and development, offering ample opportunities for career progression in a supportive environment. With competitive benefits and a commitment to employee well-being, this role not only promises meaningful work but also the chance to make a significant impact in the pharmaceutical industry.
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Contact Detail:

AbbVie Inc Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land European Regulatory Affairs Lead - Strategy & Lifecycle in Maidenhead

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of European regulations and recent changes in the biopharmaceutical landscape. We recommend creating a cheat sheet of key points to discuss, so you’re ready to impress!

✨Tip Number 3

Showcase your organisational skills! During interviews, share examples of how you've successfully managed multiple projects. We want to see how you prioritise tasks and keep everything on track.

✨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 about their job search.

We think you need these skills to ace European Regulatory Affairs Lead - Strategy & Lifecycle in Maidenhead

Regulatory Affairs
Pharmaceutical Regulations
Organizational Skills
Project Prioritisation
European Regulatory Strategy Development
Life Sciences Education
Strategic Planning
Communication Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in European Regulatory strategy development. 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 passionate about regulatory affairs and how your skills can help us implement effective registration strategies. Keep it engaging and personal!

Showcase Your Organisational Skills: Since this role involves juggling multiple projects, we’d love to see examples of how you’ve successfully managed your time and priorities in past roles. Highlight any tools or methods you use to stay organised!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates!

How to prepare for a job interview at AbbVie Inc

✨Know Your Regulations

Make sure you brush up on the latest European pharmaceutical regulations. Being able to discuss specific regulations and how they impact registration strategies will show that you’re not just familiar with the basics, but that you’re genuinely engaged with the field.

✨Showcase Your Organisational Skills

Prepare examples of how you've successfully managed multiple projects in the past. Use the STAR method (Situation, Task, Action, Result) to structure your responses, highlighting your ability to prioritise effectively under pressure.

✨Demonstrate Strategic Thinking

Think about how you would approach developing a regulatory strategy for a new product. Be ready to discuss your thought process and any relevant experiences that showcase your strategic mindset in regulatory affairs.

✨Prepare for Travel Questions

Since the role involves travel, be prepared to discuss your flexibility and willingness to travel. Share any previous experiences where travel was a part of your job and how you managed it alongside your responsibilities.

European Regulatory Affairs Lead - Strategy & Lifecycle in Maidenhead
AbbVie Inc
Location: Maidenhead
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  • European Regulatory Affairs Lead - Strategy & Lifecycle in Maidenhead

    Maidenhead
    Full-Time
    36000 - 60000 £ / year (est.)
  • A

    AbbVie Inc

    10000+
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