Regulatory Affairs

Regulatory affairs professionals ensure that products meet all necessary legal and scientific requirements for approval and market access. This includes preparing and submitting documentation, managing licences and liaising with regulatory authorities to support product development and lifecycle management.

Regulatory affairs roles are found across pharmaceuticals, biotechnology, medical devices, diagnostics and consumer health. Each sector has unique regulatory requirements, offering diverse career paths for professionals with specialised knowledge.

Most roles require a degree in life sciences, pharmacy or a related field. Experience in regulatory submissions, dossier preparation and knowledge of global regulatory frameworks (e.g. EMA, FDA, MHRA) is highly valued. Senior roles may require postgraduate qualifications or specialised certifications.

Yes. Our regulatory affairs team includes specialists with deep knowledge of global regulations and submission processes. You’ll be supported by someone who understands your discipline and can match your experience to the right opportunity.

We do. You will receive tailored interview preparation, insights into the hiring company and advice on how to present your regulatory experience effectively. We help you navigate each step with confidence and clarity.

Some roles may involve travel, especially those that include global regulatory submissions, inspections, or cross-functional collaboration. However, many positions offer remote or hybrid flexibility depending on the organisation.