Senior Manager, Global Regulatory Affairs

JR United Kingdom; Chester; On-site; GBP 60,000 - 80,000; Full time

Job summary

A global biopharmaceutical company seeks a Senior Manager in Regulatory Affairs to join their team in Chester. This position emphasizes international market strategies, requiring extensive experience in regulatory affairs within emerging markets. Ideal candidates will lead project teams and ensure compliance across various regions, impacting healthcare access substantially.

Qualifications

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

Responsibilities

• Shaping submission strategies and ensuring compliance across diverse markets.
• Playing a strategic role in the global regulatory project team.
• Supporting lifecycle management of key marketed products.

Skills

Regulatory Affairs

Cross-functional Collaboration

Submission Strategies

International Regulatory Requirements

Job description

Social network you want to login/join with:

Senior Manager, Global Regulatory Affairs, Chester

Client:

Planet Pharma

Location:

Chester, 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]