Contract: Permanent, Full Time

Salary expectations: up to £35,000 Full Time Per Annum, DOE.

A part time role may also be considered.

We are seeking a highly organised and detail-oriented Quality Associate to support our Clinical Compliance Manager and Qualified Person for Pharmacovigilance (QPPV). This is a non-technical role, ideal for someone with 1–2 years' experience in a quality-focused position, preferably within the pharmaceutical or healthcare industry.

A degree in health or pharmaceutical sciences would be preferrable but if not, then a minimum of 1-2 years' experience is required.

The successful candidate will play a key role in maintaining our Quality Management System (QMS), supporting audits, document control, and ensuring compliance with ISO 9001, Good Pharmacovigilance Practice (GVP), and regulatory requirements. Full training will be provided to build and strengthen ISO 9001 knowledge where required.

Patient safety and compliance are at the very heart of everything we do, and the Quality Associate will work collaboratively with internal teams, clients, and external stakeholders to ensure the highest quality standards are maintained.

We are unable to offer visa sponsorship.

Applicants must have the unrestricted right to live and work in the UK.

Closing date: 31 January 2026