Senior Manager, Global Regulatory Affairs

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

Job summary

A global biopharmaceutical company is seeking a Senior Manager in Global Regulatory Affairs in Cheltenham. The role involves strategic responsibilities supporting regulatory compliance in international markets, requiring significant experience in regulatory affairs. This position offers high visibility and the ability to contribute to healthcare access in underserved regions.

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

• Play a strategic role in shaping submission strategies.
• Ensure compliance across diverse markets.
• Support lifecycle management of key marketed products.

Skills

Regulatory Affairs

Cross-functional collaboration

Compliance

International regulatory requirements

Job description

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Senior Manager, Global Regulatory Affairs, Cheltenham

Client:

Planet Pharma

Location:

Cheltenham

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’ 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]