Senior Manager, Global Regulatory Affairs

JR United Kingdom; Kingston upon Hull; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global biopharmaceutical company seeks a Senior Manager for Regulatory Affairs to enhance its team in Kingston upon Hull. This role emphasizes strategic submission management and compliance in international markets. Ideal candidates have extensive experience in regulatory affairs and collaboration with cross-functional teams.

Qualifications

• Minimum of 5 years in Regulatory Affairs, focusing on International/Emerging Markets.
• Proven ability to represent the region on cross-functional teams.
• Experience in preparing NDA submissions for the IGM region.

Responsibilities

• Strategic role in submission strategies and compliance.
• Support lifecycle management of marketed products.
• Contribute to healthcare access in underserved regions.

Skills

Regulatory Affairs

International Regulatory Requirements

Cross-functional Collaboration

Job description

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Senior Manager, Global Regulatory Affairs, Kingston upon Hull, East Yorkshire

Client:

Planet Pharma

Location:

Kingston upon Hull, East Yorkshire, 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 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 will play a strategic role in shaping submission strategies and ensuring compliance across diverse markets. If you have 3–5+ years of 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 an international scope, high visibility, and the chance to contribute to healthcare access across underserved regions.

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