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Regulatory Partner
Role Overview
You will apply your regulatory and scientific expertise to influence strategic initiatives, support business decision-making, and ensure compliance in a rapidly evolving regulatory landscape. You will work closely with internal and external stakeholders, act as a key liaison with the MHRA, and contribute to both clinical and national licensing activities.
Company Information
Zenopa have partnered with a global diagnostics company with a major UK presence. They develop diagnostic tests, instruments and digital solutions used around the world to help prevent, diagnose and monitor diseases.
Their culture emphasises integrity, courage and passion, and they aim to foster an inclusive working environment where people are supported, valued and encouraged to collaborate and innovate.
Role Requirements
Lead and contribute to regulatory strategies across UK submissions, national licensing applications, clinical trial applications, and early access routes.
Serve as a primary point of contact for interactions with the MHRA, supporting negotiations and effective cross-functional communication.
Translate evolving UK regulatory requirements into internal policies, procedures, and solutions that ensure compliance and enable value creation.
Support national components of centrally authorised products and coordinate activities with global regulatory teams.
Provide strategic and technical advice to internal teams on complex regulatory issues affecting the wider business.
Person Specifications
Scientific degree (or equivalent experience) with strong understanding of technical and scientific concepts.
Extensive experience within UK Regulatory Affairs, including proven ability to navigate post-Brexit submission requirements.
Demonstrated ability to develop, implement, and communicate effective regulatory strategies.
Package
Strong basic.
Car allowence.
Pension.
Shares options.
Others to be discussed.
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Locations
We aim to operate and maintain the following set of core values