Senior Manager, Global Regulatory Affairs

JR United Kingdom; Lincoln; On-site; GBP 70,000 - 90,000; Full time

Job summary

A global biopharmaceutical company is seeking a Senior Manager for Global Regulatory Affairs to enhance its regulatory team in Lincoln. This role involves important strategic responsibilities, focusing on international growth markets and collaboration with stakeholders worldwide. Ideal candidates will have significant experience in regulatory affairs within emerging markets and the ability to drive compliance and submissions in various regions. The position promises a substantial impact on healthcare accessibility.

Qualifications

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

Responsibilities

• Shape submission strategies for regulatory compliance.
• Collaborate with global stakeholders across diverse markets.
• Manage lifecycle of key marketed products.

Skills

Regulatory Affairs

International Markets

Cross-functional collaboration

Compliance

Job description

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Senior Manager, Global Regulatory Affairs, Lincoln

Client:

Planet Pharma

Location:

Lincoln, 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 is 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 of 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]