Senior Manager, Global Regulatory Affairs

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

Job summary

A leading global biopharmaceutical company seeks a Senior Manager for Global Regulatory Affairs based in Swindon. This strategic role involves shaping submission strategies and ensuring compliance in diverse international markets, offering a significant opportunity for experienced professionals looking to advance in their careers. The position requires strong regulatory affairs expertise, particularly within emerging markets, and involves collaboration with global stakeholders.

Qualifications

• Minimum of 5 years of experience in the pharmaceutical or biotechnology industry.
• Proven ability to represent the region on cross-functional teams.
• Experience with New Drug Application submissions for the IGM region.

Responsibilities

• Shape submission strategies and ensure compliance across markets.
• Support the lifecycle management of key marketed products.
• Contribute to healthcare access in underserved regions.

Skills

Regulatory Affairs

Cross-functional Collaboration

International Regulatory Requirements

Job description

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Senior Manager, Global Regulatory Affairs, Swindon, Wiltshire

Client:

Planet Pharma

Location:

Swindon, Wiltshire, 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 is currently working on an exciting opportunity with a global biopharmaceutical company that aims 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 will play a strategic role in shaping submission strategies and ensuring compliance across diverse markets. Candidates should have 3–5+ years of experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with global stakeholders. This position offers a fantastic next step for such professionals.

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.
• Experience in preparing New Drug Application (NDA) submissions for countries within the IGM region.
• Strong understanding of international regulatory requirements and processes.

This position offers an international scope, high visibility, and the chance to contribute to healthcare access in underserved regions.

For more information or to apply, please contact Ollie at Planet Pharma at [emailprotected].