Europe Regulatory Affairs Project Lead

AbbVie; Taplow; On-site; GBP 50,000 - 70,000; Full time

Job summary

A leading global biopharmaceutical company in the UK is seeking a Regulatory Affairs professional to implement regulatory strategies and manage product compliance. The role involves interfacing with commercial teams and health authorities, as well as supporting the drug development strategy. The ideal candidate should have a strong understanding of regulatory requirements in Europe, proven experience in lifecycle management, and the ability to lead regulatory submissions effectively.

Qualifications

• Experience in regulatory strategies for pharmaceutical products.
• Strong understanding of EU and non-EU regulatory environments.
• Ability to manage product lifecycle and compliance.

Responsibilities

• Implement regulatory strategies for a portfolio of products.
• Manage submissions and lifecycle for compliance.
• Interface with brand teams and local health authorities.

Skills

Regulatory compliance

Knowledge of regulatory procedures

Leadership skills

Strategic planning

Communication skills

Job description

A leading global biopharmaceutical company in the UK is seeking a Regulatory Affairs professional to implement regulatory strategies and manage product compliance. The role involves interfacing with commercial teams and health authorities, as well as supporting the drug development strategy. The ideal candidate should have a strong understanding of regulatory requirements in Europe, proven experience in lifecycle management, and the ability to lead regulatory submissions effectively.