Head of Regulatory and Scientific Affairs

1 day ago

Surrey, United Kingdom Northreach Full time

Northreach have partnered with an exciting pharma company based in the UK that are recruiting for a Global Head of regulatory Affairs to join their team. As the Global Head of Regulatory Affairs, you will play a pivotal role in shaping the future of our products, leading regulatory strategies across all stages of development and lifecycle management. This is more than just a leadership position—it’s an opportunity to inspire and empower a talented regulatory team while building meaningful connections with global health authorities. With your vision and expertise, you’ll ensure our work not only meets but exceeds international standards, driving impactful outcomes for patients worldwide. Develop and implement innovative global regulatory strategies, ensuring compliance with local and international regulations.
Advise leadership on best practices, recommend system improvements, and drive business growth.
Act as a strategic partner to the business, supporting objectives and due diligence activities.
Oversee preparation, submission, and management of regulatory documents (INDs, NDAs, MAAs, etc.) Serve as the primary liaison with regulatory bodies, fostering communication to ensure timely approvals.
Strengthen cross-functional collaboration with internal teams and external partners to align with regulatory strategies.
Build and lead the regulatory team, fostering a culture of trust, communication, and high performance.
Identify regulatory risks and develop mitigation strategies.

Internal: Medical, operations, portfolio optimization, M&A, supply chain, commercial, finance, HR.
Suppliers, manufacturers, partners, regulatory authorities.
Master’s or doctoral degree in biology, chemistry, pharmacy, or related life sciences field.

Extensive global regulatory affairs experience in pharmaceutical, biotech, or medical device industries.
Experience in regulatory agency interactions, including MHRA and EMA;

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