Senior Manager, Global Regulatory Affairs

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

Job summary

A global biopharmaceutical company is seeking a Senior Manager in Regulatory Affairs to enhance its team in Milton Keynes. This strategic role focuses on international markets, requiring deep expertise in regulatory processes and collaboration with a cross-functional team. Candidates should have a proven track record in the pharmaceutical sector, especially in emerging markets, and aim to improve healthcare access in underserved regions. The position offers significant visibility and the chance to impact important healthcare initiatives.

Qualifications

• Minimum 5 years of experience in pharmaceutical or biotechnology industry with Regulatory Affairs focus.
• Experience with New Drug Application (NDA) submissions.
• Ability to represent the IGM group on project teams.

Responsibilities

• Shape submission strategies for key marketed products.
• Ensure compliance across diverse markets.
• Support lifecycle management in International Growth Markets.

Skills

Regulatory Affairs

Cross-functional collaboration

International regulatory requirements

Job description

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Senior Manager, Global Regulatory Affairs, Milton Keynes

Client:

Planet Pharma

Location:

Milton Keynes

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'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 would 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]