Senior Regulatory Affairs Associate

TN United Kingdom; London; On-site; GBP 40,000 - 80,000; Full time

Job summary

An innovative biotechnology company is seeking a Senior Regulatory Affairs Associate to join their pioneering team in London. This role offers a unique opportunity to support the regulatory aspects of life-changing medicines, focusing on EU submissions and product lifecycle activities. With a commitment to transforming genetic discoveries, the company provides a collaborative environment for professional growth and development. Join a dedicated team that values work-life balance and offers a competitive salary in a thriving industry.

Qualifications

• 1-2 years of regulatory affairs experience required.
• Experience with EMA submissions and EU regulatory processes.

Responsibilities

• Provide regulatory affairs support for development programs.
• Assist with EU submissions for PRIME and Orphan Drug Designation.

Skills

Regulatory Affairs

EMA Submissions

Clinical Experience

EU Submissions

Education

Bachelor's Degree

Job description

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Senior Regulatory Affairs Associate, London

Client:

Location:

London, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

Job Reference:

c62027ba4a67

Job Views:

5

Posted:

05.05.2025

Expiry Date:

19.06.2025

Job Description:

Your new company

Are you ready to join a pioneering team in the biotechnology industry? We are a global leader dedicated to transforming genetic discoveries into life-changing medicines. Our innovative approach targets the root causes of genetic conditions, offering hope and improved health outcomes to patients worldwide. This is a great opportunity to join a loyal and high-growth team that has been in business for a minimum of 8 years.

Your new role

You will be joining as a Senior Regulatory Affairs Associate. This position focuses on providing regulatory affairs support to both ongoing development programs and approved product lifecycle activities. You will support the EU Lead regarding planning, assist with the development of the EU submissions for PRIME and Orphan Drug Designation, and ATMP classification. This is a great opportunity to grow both as an individual and as a regulatory professional.

What you'll need to succeed

EU, early-stage, and clinical experience, EMA submissions. You will have a minimum of 1–2 years of regulatory affairs experience.

What you'll get in return

You will enjoy a good work-life balance, opportunities to grow and develop under excellent leadership, and a competitive market salary.