Senior Manager, Regulatory Affairs UK & Ireland

Biogen; Guide Post; Hybrid; GBP 80,000 - 100,000

Job description

Senior Manager, Regulatory Affairs UK & Ireland

Biogen Guide Post, England, United Kingdom

Job Description

About This Role
Joining us as a Senior Manager, Regulatory Affairs UK & Ireland, you will be responsible for supporting and maintaining country-specific regulatory and R&D compliance activities across our pipeline and product portfolio, in line with the company’s strategy and the management of benefit/risk activities. You will play a key role driving regulatory strategies in alignment with business objectives, in addition to ensuring compliance.

In this role you will work closely with the in-country Regulatory Head, Global Regulatory Affairs colleagues and R&D teams, as well as with various local functions such as Medical, Marketing, Market Access and Quality Assurance. You will have close interactions with external regulatory authorities, advisory committees and cooperative groups.

This is a hybrid role, requiring attendance at our Maidenhead offices 2-3 days per week.

What You’ll Do

• Lead and support local regulatory activities for the UK/Ireland affiliate, reporting through the Global Regulatory Affairs (GRA) group.
• Manage pre- and post-approval procedures for pipeline and marketed products, including orphan applications, ILAP, PIPs, Scientific Advice, EAMs, MAA filings, and post-approval maintenance.
• Oversee local labelling processes and ensure timely updates for centralized products in Ireland.
• Review and approve packaging, artwork, and educational materials.
• Maintain strong relationships with regulatory authorities, advisory committees, and industry groups.
• Monitor and provide insights on regulatory intelligence to support business strategy.
• Ensure operational compliance with in-country regulatory responsibilities.
• Represent Biogen in local trade associations and regulatory groups as needed.

Who You Are
You are an experienced regulatory affairs professional with strong experience in the UK and Ireland regulatory landscape. You excel at working collaboratively across teams, building relationships with key stakeholders, and ensuring regulatory compliance. You have a strategic mindset and the ability to navigate complex regulatory requirements effectively.

Qualifications

Required Skills

• Strong and proven experience in Regulatory Affairs within the (bio)pharmaceutical industry.
• Strong understanding of UK and Ireland regulatory frameworks.
• An excellent communicator, with the ability to lead strategic cross functional team discussions.
• Proficiency in MS Office, regulatory databases (e.g., Cortellis), and electronic document management systems.
• Ability to work independently and manage multiple priorities.

Additional Information

Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Legal, Research, and Science
• Industries: Biotechnology Research, Pharmaceutical Manufacturing, and Research Services