Regulatory Affairs Executive - Pharmaceutical

Regulatory Affairs Executive - Pharmaceutical

On-site | Permanent role | £32,000pa

An exciting opportunity has arisen for an experienced Regulatory Affairs Executive to join a busy and collaborative pharmaceutical regulatory team.

This role will see you managing a varied portfolio of UK licences, taking ownership of submissions and ensuring ongoing compliance across the product lifecycle. You'll work closely with internal stakeholders and act as a subject matter expert, supporting both routine and complex licensing activities.

You’ll be responsible for the end‑to‑end preparation, submission and follow‑up of:

• New PLPI licence applications
• Variations and change notifications
• Licence renewals

You’ll liaise directly with the MHRA, maintain accurate regulatory data, ensure GMP documentation is completed to a high standard and proactively monitor regulatory changes. The role also includes involvement in continuous improvement initiatives and, when required, deputising for senior regulatory colleagues.

• Managing and maintaining your own licence portfolio
• Preparing high‑quality regulatory submissions with a strong first‑time approval focus
• Acting as a key regulatory contact for internal teams, including commercial and purchasing
• Identifying and assessing regulatory changes and supporting implementation
• Contributing to process improvements and departmental projects
• Ensuring excellent customer service and clear communication at all levels

• Previous experience in Pharmaceutical Regulatory Affairs.
• Good working knowledge of GMP and UK regulatory requirements.
• Strong written and verbal communication skills with excellent attention to detail.
• Confident stakeholder management and problem‑solving ability.
• A proactive, organised and collaborative approach.

A scientific degree is desirable (pharmaceutical sciences preferred), along with experience of regulatory documentation and quality systems.

This is a great opportunity to take real ownership within a supportive regulatory environment, with exposure to a broad range of licensing activities and the chance to influence process improvement and best practice.

If you’re looking to progress your regulatory career in a hands‑on, varied role, we’d love to hear from you.