Regulatory Affairs Executive - Pharmaceutical

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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 implementation Contributing to process improvements and departmental projects Ensuring excellent customer service and clear communication at all levels
The ideal candidate for the Regulatory Affairs Executive role will have the following background
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. Why apply? 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. Keywords: Regulatory Affairs Executive, Regulatory Affairs, RA, Regulatory #J-18808-Ljbffr
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Location:
Bolton
Job Type:
FullTime

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