Senior Manager, Global Regulatory Affairs

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

Job summary

A leading biopharmaceutical company is seeking a Senior Manager in Global Regulatory Affairs to join their team in Ipswich. In this role, you will be pivotal in shaping international submission strategies and managing compliance across diverse markets. Ideal candidates will have significant experience in regulatory affairs within the pharmaceutical industry, particularly in emerging markets, and demonstrate strong collaboration skills.

Qualifications

• Minimum of 5 years’ experience in the pharmaceutical or biotechnology industry, focusing on Regulatory Affairs.
• Experience in preparing New Drug Application (NDA) submissions.
• Strong understanding of international regulatory processes.

Responsibilities

• Shape submission strategies for regulatory compliance.
• Support lifecycle management of key marketed products.
• Represent the International/Global Markets group on cross-functional teams.

Skills

Regulatory Affairs

Cross-functional collaboration

International regulatory requirements

Job description

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Senior Manager, Global Regulatory Affairs, Ipswich

Client:

Planet Pharma

Location:

Job Category:

Other

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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’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]