Senior Manager, Global Regulatory Affairs

JR United Kingdom; Bournemouth; On-site; GBP 70,000 - 100,000; Full time

Job summary

Une entreprise biopharmaceutique mondiale recherche un Senior Manager pour son équipe d'affaires réglementaires à Bournemouth. Le poste nécessite une expérience significative en affaires réglementaires, particulièrement dans les marchés internationaux, et offre une occasion de contribuer à l'accès aux soins de santé dans des régions mal desservies.

Qualifications

• Minimum de 5 ans d'expérience dans l'industrie pharmaceutique ou biotechnologique.
• Expérience dans le traitement des soumissions NDA pour le marché international.
• Capacité à collaborer avec des parties prenantes mondiales.

Responsibilities

• Jouer un rôle stratégique dans les projets réglementaires globaux.
• Soutenir la gestion du cycle de vie des produits commercialisés.
• Représenter la région sur des équipes de projet transversales.

Skills

Cross-functional collaboration

Regulatory Affairs

International Regulatory Requirements

Job description

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Senior Manager, Global Regulatory Affairs, Bournemouth

Client:

Planet Pharma

Location:

Bournemouth, 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’d 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]