Senior Manager, Global Regulatory Affairs

JR United Kingdom; Chelmsford; On-site; GBP 80,000 - 120,000; Full time

Job summary

A global biopharmaceutical company is looking for a Senior Manager in Global Regulatory Affairs in Chelmsford. This pivotal role involves shaping submission strategies for key products in International Growth Markets, requiring a strong background in Regulatory Affairs and collaboration with global stakeholders. This opportunity offers high visibility and the chance to impact healthcare access.

Qualifications

• Minimum of 5 years of experience in the pharmaceutical or biotechnology industry.
• Experience in preparing New Drug Application (NDA) submissions is essential.
• Proven ability to represent the region on cross-functional project teams.

Responsibilities

• Play a strategic role in submission strategies for international markets.
• Ensure compliance across diverse markets.
• Contribute to meaningful healthcare access across underserved regions.

Skills

Regulatory Affairs

Cross-functional Collaboration

International Regulatory Requirements

Job description

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Senior Manager, Global Regulatory Affairs, Chelmsford

Client:

Planet Pharma

Location:

Chelmsford

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. 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].