Senior Manager Global Regulatory Affairs in London
Senior Manager Global Regulatory Affairs

Senior Manager Global Regulatory Affairs in London

London Full-Time 48000 - 72000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead regulatory activities for international markets and support product expansions.
  • Company: Join a global pharmaceutical leader with a focus on innovation.
  • Benefits: Permanent role with hybrid working and opportunities for career growth.
  • Why this job: Make a real impact in global healthcare by managing regulatory affairs.
  • Qualifications: Degree in life sciences and 5+ years in international regulatory experience.
  • Other info: Collaborative team environment with a focus on strategic development.

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

Blackfield Associates are proudly partnered with an international pharmaceutical client on an exclusive basis, who are looking to establish a new team for their international and emerging markets division. We’re looking for an experienced Regulatory Manager to execute activities across international markets and EMEA. This includes submission and maintenance of new products, both generic and speciality, as well as supporting the global expansion of existing products.

As Regulatory Affairs Manager, you will:

  • Preparation and submission of new marketing authorisation applications, supporting international countries within the EMEA region
  • Preparation and submission of registrations for existing products as part of global expansion activities
  • Lead dossier remediation activities, such as aligning older registrations with current regulatory requirements in support of geographic expansion
  • Support lifecycle management activities for marketed products, including Variations, Renewals and PSURs
  • Liaise with local Regulatory Affairs staff on regulatory documentation, including labelling, variations, and new registrations
  • Support local Regulatory Affairs teams with countries-specific labelling activities
  • Track registrations using relevant regulatory databases and tracking systems
  • Maintain regulatory archives, including dossiers, documents, and media
  • Provide regulatory support to cross‑functional teams (portfolio management, out‑licensing, launch management)
  • Proactively contribute to the strategic development of the Regulatory Affairs function and support the successful commercial development of international markets within the EMEA region

To be considered for the role of Regulatory Affairs Manager, you will have:

  • Educated to degree level in relevant life sciences studies
  • Minimum 5 years’ experience supporting international markets
  • Previous experience managing New MAA’s, Global expansion of existing products and extensive lifecycle maintenance is essential
  • Experience working closely with international Regulatory Affairs affiliates
  • Strong ability to manage deadlines and priorities multiple projects simultaneously
  • Ability to work independently and collaboratively within a team environment

This is a permanent, full-time role. Located at the affiliate office, you will need to be able to attend the Slough office on a hybrid basis. Unable to sponsor, candidates must have full right to work in the UK and flexibility around working hours due to territories.

Senior Manager Global Regulatory Affairs in London employer: Blackfield Associates

Join a dynamic and innovative international pharmaceutical company that prioritises employee development and fosters a collaborative work culture. With a focus on regulatory excellence, you will have the opportunity to lead impactful projects across EMEA while enjoying a hybrid working model that promotes work-life balance. Our commitment to your growth is reflected in our supportive environment, where your contributions directly influence the global expansion of our product portfolio.
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Contact Detail:

Blackfield Associates Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Manager Global Regulatory Affairs in London

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those in regulatory affairs. A friendly chat can lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of international regulations and recent changes in the EMEA region. We want you to impress with your expertise and show that you're the go-to person for regulatory challenges.

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you and match your skills in regulatory affairs.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit for their team.

We think you need these skills to ace Senior Manager Global Regulatory Affairs in London

Regulatory Affairs
Marketing Authorisation Applications (MAA)
Global Expansion
Lifecycle Management
Dossier Remediation
Regulatory Documentation
Labelling
Project Management
Cross-Functional Collaboration
Regulatory Databases
Attention to Detail
Deadline Management
Team Collaboration
Life Sciences Education

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the role of Senior Manager Global Regulatory Affairs. Highlight your experience with marketing authorisation applications and global expansion activities, as these are key aspects of the job.

Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of your past experiences in regulatory affairs, especially in international markets, to show how you can contribute to our team.

Showcase Your Teamwork Skills: Since collaboration is crucial in this role, make sure to mention any experiences where you've successfully worked with cross-functional teams. We want to see how you can support and enhance our regulatory function!

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 this exciting opportunity in our new team.

How to prepare for a job interview at Blackfield Associates

✨Know Your Regulatory Stuff

Make sure you brush up on the latest regulations and guidelines relevant to international markets, especially within the EMEA region. Familiarise yourself with recent changes in regulatory affairs that could impact the role, as this will show your commitment and expertise.

✨Showcase Your Experience

Prepare specific examples from your past roles where you've successfully managed new marketing authorisation applications or supported global expansion activities. Use the STAR method (Situation, Task, Action, Result) to structure your responses and highlight your achievements.

✨Demonstrate Team Collaboration

Since the role involves liaising with local Regulatory Affairs teams, be ready to discuss how you've worked collaboratively in the past. Share instances where you’ve supported cross-functional teams and how your contributions led to successful outcomes.

✨Ask Insightful Questions

Prepare thoughtful questions about the company’s regulatory strategies and future plans for international markets. This not only shows your interest in the role but also helps you gauge if the company aligns with your career goals.

Senior Manager Global Regulatory Affairs in London
Blackfield Associates
Location: London

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