Senior Manager, Global Regulatory Affairs

JR United Kingdom; High Wycombe; On-site; GBP 65,000 - 90,000; Full time

Job summary

A leading biopharmaceutical company seeks a Senior Manager for Global Regulatory Affairs in High Wycombe. This strategic role offers visibility and involves lifecycle management of marketed products, requiring a depth of experience in regulatory affairs within international markets.

Qualifications

• 5+ years of experience in pharmaceutical or biotechnology industry focusing on Regulatory Affairs.
• Experience in International or Emerging Markets is preferred.
• Strong understanding of international regulatory requirements.

Responsibilities

• Shape submission strategies and ensure compliance across diverse markets.
• Represent region and group on cross-functional project teams.
• Prepare New Drug Application (NDA) submissions for International/Global Markets.

Skills

Project Management

Cross-functional Collaboration

Regulatory Compliance

Job description

Social network you want to login/join with:

Senior Manager, Global Regulatory Affairs, High Wycombe

Client:

Planet Pharma

Location:

High Wycombe, 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’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]