Senior Manager, Global Regulatory Affairs

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

Job summary

Une position de Senior Manager dans les affaires réglementaires auprès d'une entreprise biopharmaceutique mondiale à Crawley. Le rôle implique de soutenir la gestion du cycle de vie des produits commercialisés tout en collaborant avec diverses équipes à l'échelle internationale. Le candidat idéal aura une forte expérience dans les affaires réglementaires, notamment dans les marchés émergents.

Qualifications

• Minimum de 5 ans d'expérience dans l'industrie pharmaceutique ou biotechnologique.
• Expérience dans la préparation de soumissions NDA pour la région IGM.
• Compréhension solide des exigences réglementaires internationales.

Responsibilities

• Jouer un rôle stratégique dans la définition des stratégies de soumission.
• Assurer la conformité à travers des marchés divers.
• Collaborer avec des parties prenantes mondiales.

Skills

Regulatory Affairs

Cross-functional collaboration

Compliance

Job description

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Senior Manager, Global Regulatory Affairs, Crawley, West Sussex

Client:

Planet Pharma

Location:

Crawley, West Sussex, 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]