Global Regulatory Submissions Leader in Holmfirth
Global Regulatory Submissions Leader

Global Regulatory Submissions Leader in Holmfirth

Holmfirth Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory submission projects and ensure quality delivery in a dynamic environment.
  • Company: Global biopharmaceutical leader dedicated to innovative therapies.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Make a real difference in patient outcomes through impactful work.
  • Qualifications: 10-15 years in regulatory affairs or project management, with a scientific degree.
  • Other info: Join a collaborative team focused on innovation and excellence.

The predicted salary is between 48000 - 72000 £ per year.

A global biopharmaceutical leader is seeking a Head of Regulatory Submission Project Management in the UK. This role involves leading a unified project management organization for regulatory submissions, ensuring quality and timely delivery.

Candidates should have 10-15 years of experience in regulatory affairs or project management within the pharmaceutical industry, along with a bachelor's degree in a scientific discipline.

Join us in impacting patient outcomes through innovative therapies.

Global Regulatory Submissions Leader in Holmfirth employer: Ipsen Pharma (SAS)

As a global biopharmaceutical leader, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to make a meaningful impact on patient outcomes. With a strong commitment to professional development, we offer extensive growth opportunities and a supportive environment in the UK, where you can thrive alongside industry experts dedicated to advancing healthcare through cutting-edge therapies.
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Contact Detail:

Ipsen Pharma (SAS) Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Global Regulatory Submissions Leader in Holmfirth

✨Tip Number 1

Network like a pro! Reach out to industry contacts on LinkedIn or attend relevant events. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.

✨Tip Number 2

Prepare for interviews by researching the company and its recent projects. We want to show that you’re genuinely interested in their work and how you can contribute to their mission of improving patient outcomes.

✨Tip Number 3

Practice your pitch! We recommend crafting a concise summary of your experience and how it aligns with the role. This will help you stand out when discussing your background in regulatory affairs or project management.

✨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 Global Regulatory Submissions Leader in Holmfirth

Regulatory Affairs
Project Management
Quality Assurance
Timely Delivery
Pharmaceutical Industry Knowledge
Scientific Discipline
Leadership Skills
Communication Skills
Stakeholder Management
Problem-Solving Skills
Team Collaboration
Attention to Detail
Strategic Planning
Risk Management

Some tips for your application 🫡

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

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory submissions and how your skills can help us impact patient outcomes. Keep it engaging and personal.

Showcase Your Experience: With 10-15 years of experience required, we want to see specific examples of your past projects. Highlight any successful regulatory submissions you've led and the results they achieved. Numbers speak volumes!

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 this exciting opportunity. Don’t miss out!

How to prepare for a job interview at Ipsen Pharma (SAS)

✨Know Your Stuff

Make sure you brush up on the latest trends and regulations in the biopharmaceutical industry. Familiarise yourself with the specific regulatory submission processes relevant to the role, as this will show your depth of knowledge and commitment to the field.

✨Showcase Your Experience

Prepare to discuss your past experiences in regulatory affairs or project management. Have specific examples ready that highlight your leadership skills and how you've successfully managed submissions in a timely manner. This will demonstrate your capability to lead a unified project management organisation.

✨Understand the Company’s Mission

Research the company’s innovative therapies and their impact on patient outcomes. Being able to articulate how your values align with theirs will not only impress them but also show that you’re genuinely interested in contributing to their mission.

✨Ask Insightful Questions

Prepare thoughtful questions about the team dynamics, challenges they face in regulatory submissions, and how success is measured in this role. This shows that you’re not just looking for a job, but are keen to understand how you can make a real difference.

Global Regulatory Submissions Leader in Holmfirth
Ipsen Pharma (SAS)
Location: Holmfirth

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