Senior Manager, Global Regulatory Affairs

JR United Kingdom; Nottingham; On-site; GBP 50,000 - 80,000; Full time

Job summary

A leading global biopharmaceutical company seeks a Senior Manager for their Regulatory Affairs team in Nottingham. This role involves managing regulatory compliance for key products, particularly in emerging markets, and requires strong cross-functional collaboration and a proven background in regulatory affairs. Candidates with 5+ years of experience will find this opportunity to be an impactful next step in their careers.

Qualifications

• 5+ years of experience in pharmaceutical or biotechnology industry.
• Experience in preparing NDA submissions.
• Strong understanding of international regulatory processes.

Responsibilities

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

Skills

Cross-functional collaboration

Regulatory requirements understanding

Education

Bachelor's degree in relevant field

Job description

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Senior Manager, Global Regulatory Affairs, Nottingham

Client:

Planet Pharma

Location:

Nottingham, 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’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’ll 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]