UK Regulatory Affairs Lead - Strategy & Submissions in Maidenhead
UK Regulatory Affairs Lead - Strategy & Submissions

UK Regulatory Affairs Lead - Strategy & Submissions in Maidenhead

Maidenhead Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory activities and submissions for a top pharmaceutical company.
  • Company: A leading pharmaceutical firm based in Maidenhead with a collaborative culture.
  • Benefits: Competitive salary, career development opportunities, and a supportive work environment.
  • Why this job: Shape regulatory strategy and ensure compliance while making a real impact.
  • Qualifications: Strong background in regulatory submissions and line management experience.
  • Other info: Join a dynamic team and advance your career in the pharmaceutical industry.

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

A leading pharmaceutical company in Maidenhead seeks an experienced Regulatory professional to act as the primary contact responsible for regulatory activities in the UK. The ideal candidate has a strong background in regulatory submissions, line management experience, and excellent interpersonal skills. This role offers the opportunity to guide regulatory strategy and ensure compliance with national and EU legislation while working in a collaborative environment.

UK Regulatory Affairs Lead - Strategy & Submissions in Maidenhead employer: AbbVie Inc

As a leading pharmaceutical company based in Maidenhead, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. With a strong focus on professional development, we offer numerous growth opportunities and support for continuous learning, ensuring that our team members can thrive in their careers while making a meaningful impact in the healthcare sector.
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Contact Detail:

AbbVie Inc Recruiting Team

StudySmarter Expert Advice 🤫

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

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs 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 UK and EU regulations. We want you to showcase your expertise in regulatory submissions and strategy, so be ready to discuss real-life scenarios where you've navigated compliance challenges.

✨Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It shows professionalism and keeps you fresh in their minds.

✨Tip Number 4

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 right from the start.

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

Regulatory Submissions
Line Management
Interpersonal Skills
Regulatory Strategy
Compliance Knowledge
National Legislation Understanding
EU Legislation Understanding
Collaborative Working

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in regulatory submissions and line management. We want to see how your background aligns with the role, so don’t be shy about showcasing your relevant skills!

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 UK Regulatory Affairs Lead position. Share specific examples of your past successes in regulatory strategy and compliance.

Show Off Your Interpersonal Skills: Since this role involves collaboration, we’d love to see how you work with others. Mention any experiences where you’ve successfully navigated team dynamics or built strong relationships in your previous roles.

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!

How to prepare for a job interview at AbbVie Inc

✨Know Your Regulatory Stuff

Make sure you brush up on UK and EU regulatory frameworks. Familiarise yourself with recent changes in legislation and be ready to discuss how they impact submissions. This shows you're not just knowledgeable but also proactive about staying updated.

✨Showcase Your Leadership Skills

Since the role involves line management, prepare examples of how you've successfully led teams or projects in the past. Highlight your interpersonal skills by discussing how you’ve resolved conflicts or motivated team members to achieve regulatory goals.

✨Prepare for Scenario Questions

Expect questions that ask how you would handle specific regulatory challenges. Think through potential scenarios related to compliance issues or submission strategies, and be ready to articulate your thought process and decision-making.

✨Ask Insightful Questions

At the end of the interview, have a few thoughtful questions ready about the company's regulatory strategy or team dynamics. This not only shows your interest in the role but also gives you a chance to assess if the company culture aligns with your values.

UK Regulatory Affairs Lead - Strategy & Submissions in Maidenhead
AbbVie Inc
Location: Maidenhead
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  • UK Regulatory Affairs Lead - Strategy & Submissions in Maidenhead

    Maidenhead
    Full-Time
    43200 - 72000 £ / year (est.)
  • A

    AbbVie Inc

    10000+
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