Senior Manager, Global Regulatory Affairs

JR United Kingdom; Shrewsbury; On-site; GBP 60,000 - 85,000; Full time

Job summary

A global biopharmaceutical company is looking for a Senior Manager in Regulatory Affairs to join their team in Shrewsbury. This role requires 5+ years of regulatory experience, with a focus on emerging markets and international collaboration. You will shape submission strategies and ensure compliance across various markets, contributing to meaningful healthcare access.

Qualifications

• 5+ years experience in pharmaceutical/biotechnology, focusing on Regulatory Affairs.
• Experience in preparing NDA submissions for international markets.
• Strong representation skills on cross-functional teams.

Responsibilities

• Developing submission strategies for diverse international markets.
• Ensuring compliance across regions for marketed products.
• Collaborating with global stakeholders effectively.

Skills

Regulatory Affairs

Cross-functional Collaboration

Understanding of International Regulatory Requirements

Job description

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Senior Manager, Global Regulatory Affairs, Shrewsbury

Client:

Planet Pharma

Location:

Shrewsbury, United Kingdom

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]