Senior Manager, Global Regulatory Affairs

JR United Kingdom; Brighton; On-site; GBP 70,000 - 100,000; Full time

Job summary

A global biopharmaceutical company is looking for a Senior Manager in Global Regulatory Affairs in Brighton. This role will be crucial in overseeing submission strategies and ensuring regulatory compliance across international markets. Candidates should have significant experience in regulatory affairs, particularly within emerging markets, and be skilled in cross-functional collaboration.

Qualifications

• Minimum of 5 years in pharmaceutical or biotechnology industry focused on Regulatory Affairs.
• Experience preparing New Drug Application (NDA) submissions for IGM countries.
• Strong understanding of international regulatory requirements.

Responsibilities

• Play a strategic role in shaping submission strategies.
• Ensure compliance across diverse markets.
• Represent the region on cross-functional project teams.

Skills

Regulatory Affairs

Cross-functional Collaboration

International Regulatory Requirements

Job description

Senior Manager, Global Regulatory Affairs, brighton

Client:

Planet Pharma

Location:

brighton, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

Job Views:

3

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

Planet Pharma are currently working on an exciting opportunity with a global biopharmaceutical company that’s looking to expand its Regulatory Affairs team. The role focuses on International Growth Markets, supporting the lifecycle management of key marketed products.

As a key member of the global regulatory project team, you’d play a strategic role in shaping submission strategies and ensuring compliance across diverse markets. If you have 3–5+ years’ experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with global stakeholders, this could be a fantastic next step.

Requirements:

• Minimum of 5 years of experience in the pharmaceutical or biotechnology industry, with a focus on Regulatory Affairs—preferably within International or Emerging Markets.
• Proven ability to effectively represent the region and the International/Global Markets (IGM) group on cross-functional project teams.
• Demonstrated experience in preparing New Drug Application (NDA) submissions for countries within the IGM region.
• Strong understanding of international regulatory requirements and processes.

The position offers a truly international scope, high visibility, and the chance to contribute to meaningful healthcare access across underserved regions.

For more information or to apply, please contact Ollie at Planet Pharma at [e-mail]

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Created on 04/06/2025 by JR United Kingdom