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.

The role

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.

Key responsibilities for the Regulatory Affairs Executive role:

* 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 implem...