Senior Manager, Global Regulatory Affairs

JR United Kingdom; Stevenage; On-site; GBP 60,000 - 90,000; Full time

Job summary

A leading global biopharmaceutical company seeks a Senior Manager for their Regulatory Affairs team in Stevenage. This strategic role involves managing submission strategies and ensuring compliance across international markets, particularly within emerging regions. Candidates should have over 5 years of Regulatory Affairs experience, especially in pharma or biotech, and demonstrate strong cross-functional collaboration skills.

Qualifications

• 5+ years in pharmaceutical/biotechnology industry focused on Regulatory Affairs.
• Experience with New Drug Application submissions.
• Strong understanding of international regulatory requirements.

Responsibilities

• Support lifecycle management of key marketed products.
• Shape submission strategies as part of the global regulatory project team.
• Ensure compliance across diverse international markets.

Skills

Cross-functional collaboration

Regulatory compliance

Strategic submission planning

Job description

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Senior Manager, Global Regulatory Affairs, Stevenage

Client: Planet Pharma

Location: Stevenage

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]