Senior Manager, Global Regulatory Affairs

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

Job summary

A global biopharmaceutical company seeks a Senior Manager for Regulatory Affairs in Telford. This role emphasizes strategic development in international markets and requires at least five years of experience in the pharmaceutical industry. The position offers visibility and the chance to impact healthcare access across underserved regions.

Qualifications

• Minimum of 5 years in pharmaceutical or biotechnology focusing on Regulatory Affairs.
• Experience preparing New Drug Application (NDA) submissions.
• Proven ability to represent on cross-functional project teams.

Responsibilities

• Shape submission strategies for diverse markets.
• Ensure compliance with international regulatory processes.
• Collaborate with global stakeholders in regulatory project teams.

Skills

Regulatory Affairs

Cross-functional Collaboration

International Regulatory Requirements

Job description

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Senior Manager, Global Regulatory Affairs, Telford

Client:

Planet Pharma

Location:

Telford, 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 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. The ideal candidate will have 3–5+ years of experience in regulatory affairs, particularly in emerging markets, and enjoy cross-functional collaboration with global stakeholders.

Requirements:

• Minimum of 5 years of experience in the pharmaceutical or biotechnology industry, focusing on Regulatory Affairs—preferably within International or Emerging Markets.
• Proven ability to represent the region and the International/Global Markets (IGM) group on cross-functional project teams.
• 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 an international scope, high visibility, and the chance to contribute to healthcare access across underserved regions.

For more information or to apply, please contact Ollie at Planet Pharma at [emailprotected].