Quality Associate (full time) - Permanent, Milton Keynes
Salary 28-35K DOE
Our client is a market leader within the Pharmacovigilance sector
They are seeking to recruit a highly organised and detail-oriented Quality Associate to support their 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.
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 our client does, and the Quality Associate will work collaboratively with internal teams, clients, and external stakeholders to ensure the highest quality standards are maintained.
*Unfortunately they are unable to offer visa sponsorship.