Senior Manager, Global Regulatory Affairs

JR United Kingdom; Northampton; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Senior Manager for its Global Regulatory Affairs team in Northampton. This role involves shaping submission strategies and ensuring compliance in emerging markets, offering international visibility and the chance to improve healthcare access across underserved regions. If you have significant experience in regulatory affairs and enjoy teamwork across borders, this could be the perfect opportunity.

Qualifications

• 5+ years of experience in pharmaceutical or biotechnology industry.
• Experience with NDA submissions in International/Emerging Markets.
• Strong understanding of international regulatory processes.

Responsibilities

• Play a strategic role in shaping submission strategies.
• Ensure compliance across diverse international markets.
• Collaborate with global stakeholders.

Skills

Regulatory Affairs

Cross-functional collaboration

International regulatory requirements

Education

Bachelor's degree in life sciences

Job description

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Senior Manager, Global Regulatory Affairs, Northampton

Client:

Planet Pharma

Location:

Northampton, 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 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 great 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.
• 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]