Senior Manager, Global Regulatory Affairs

JR United Kingdom; Bristol; On-site; GBP 60,000 - 90,000; Full time

Job summary

A global biopharmaceutical company is seeking a Senior Manager for Global Regulatory Affairs based in Bristol. The position involves ensuring compliance and supporting the lifecycle management of healthcare products in international markets. Ideal candidates will have extensive experience in regulatory affairs, particularly in emerging markets, playing a strategic role in enhancing global healthcare access.

Qualifications

• 5+ years of experience in Regulatory Affairs within pharmaceuticals or biotechnology.
• Experience with New Drug Application (NDA) submissions.
• Strong understanding of international regulatory requirements.

Responsibilities

• Support lifecycle management of key marketed products.
• Shape submission strategies across diverse markets.
• Collaborate with global stakeholders on regulatory projects.

Skills

Regulatory Affairs

Cross-functional Collaboration

International Regulatory Requirements

Job description

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Senior Manager, Global Regulatory Affairs, bristol

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Client:

Planet Pharma

Location:

bristol, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

04.06.2025

Expiry Date:

19.07.2025

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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 [emailprotected]