Senior Manager, Global Regulatory Affairs

JR United Kingdom; Chesterfield; On-site; GBP 70,000 - 95,000; Full time

Job summary

A leading biopharmaceutical company seeks a Senior Manager for Global Regulatory Affairs in Chesterfield. This strategic role includes shaping submission strategies and collaborating across global teams to enhance healthcare access in emerging markets. Ideal candidates have 5+ years' experience in regulatory affairs, particularly in international settings.

Qualifications

• Minimum 5 years experience in pharmaceutical/biotechnology industry focusing on Regulatory Affairs.
• Experience in preparing NDA submissions for International/Growth Markets.
• Proven ability to represent the region on cross-functional teams.

Responsibilities

• Shape submission strategies and ensure compliance for key products.
• Support lifecycle management in International Growth Markets.
• Play a strategic role in global regulatory project team.

Skills

Regulatory Affairs

Cross-functional collaboration

International regulatory requirements

Job description

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Senior Manager, Global Regulatory Affairs, chesterfield

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Client:

Planet Pharma

Location:

chesterfield, 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]